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for invention","granted":true,"earliest_filing_date":"2005-03-01","grant_date":"2010-03-09","anticipated_term_date":"2025-09-04","discontinuation_date":"2018-04-09","has_disclaimer":false,"patent_status":"INACTIVE","publication_count":2,"has_spc":false,"has_grant_event":false,"has_entry_into_national_phase":false},"abstract":{"en":[{"text":"Novel benzenedicarboxamides of the formula (I) wherein X represents hydrogen, halogen atom, nitro, C 1-6 alkylsulfonyloxy, C 1-6 alkylsulfinyl, C 1-6 alkylsulfenyl or C 1-6 alkylsulfonyl, R 1 represents C 1-6 alkyl, C 1-6 alkylthio-C 1-6 alkyl, or C 1-6 alkyl, m represents 0 or 1, A represents O, S, SO, SO 2 , CH 2 or CH(CH 3 ), and Q represents a 5- or 6-membered heterocyclic group that contains at least one hetero atom selected from the group consisting of N, O and S and can be optionally substituted; processes for their preparation, their intermediates and their use as insecticides.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"abstract_lang":["en"],"has_abstract":true,"claim":{"en":[{"text":"1. A compound of formula (I) wherein X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, C 1-4 alkylsulfonyloxy, C 1-4 alkylsulfinyl, C 1-4 alkylsulfenyl or C 1-4 alkylsulfonyl, R 1 represents C 1-4 alkyl, C 1-4 alkylthio-C 1-4 alkyl, C 1-4 alkylsulfinyl-C 1-4 alkyl or C 1-4 alkylsulfonyl- 1-4 alkyl, Y represents fluorine, chlorine, bromine or C 1-4 alkyl, m represents 1, A represents CH 2 or CH(CH 3 ), and Q represents a 5-membered or 6-membered heterocyclic group that contains one to three N-atoms and which can be optionally substituted by at least one member selected from a group consisting of C 1-6 alkyl, C 1-6 alkoxy, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, C 1-6 haloalkyl, C 1-10 haloalkoxy, C 1-6 haloalkylthio, C 1-6 haloalkylsulfinyl, C 1-6 haloalkylsulfonyl, C 1-6 haloalkylcarbonyl, halogen, oxo and hydroxy.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"2. A compound according to claim 1 wherein X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, methanesulfonyloxy, C 1-2 alkylsulfinyl, C 1-2 alkylsulfenyl or C 1-2 alkylsulfonyl, R 1 represents isopropyl, C 1-2 alkylthio-C 3-4 alkyl, C 1-2 alkylsulfinyl-C 3-4 alkyl or C 1-2 alkylsulfonyl-C 3-4 alkyl, Y represents fluorine, chlorine or methyl, m represents 1, A represents CH 2 or CH(CH 3 ), and Q represents a hetero cyclic group, selected from a group consisting of pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, and pyrimidinyl each of which may be optionally substituted by at least one member selected from the group consisting of C 1-4 alkyl, C 1-4 alkoxy, C 1-4 alkylthio, C 1-4 alkylsulfinyl, C 1-4 alkylsulfonyl, C 1-8 haloalkyl, C 1-4 haloalkoxy, C 1-4 haloalkylthio, C 1-4 haloalkylsulfinyl, C 1-4 haloalkylsulfonyl, C 1-4 haloalkylcarbonyl, fluorine, chlorine, bromine, iodine, oxo and hydroxy.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"3. A composition comprising a compound according to claim 1 and a diluent or a carrier.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"4. A composition according to claim 3 , further comprising at least one extender and/or surface active agent.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"5. A compound of formula (VIII) wherein X represents hydrogen, halogen, nitro, C 1-6 alkylsulfonyloxy, C 1-6 alkylsulfinyl, C 1-6 alkylsulfenyl or C 1-6 alkylsulfonyl, Y represents halogen or C 1-6 alkyl, A represents CH 2 or CH(CH 3 ), and Q represents a 5-membered or 6-membered heterocyclic group that contains one to three N-atoms, or one O-atom or one S-atom and can be optionally substituted.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"claim_lang":["en"],"has_claim":true,"description":{"en":{"text":"This application is a 35 U.S.C. §371 U.S. National Phase filing of International Application No. PCT/EP2005/002130, filed Mar. 1, 2005, which claims the benefit of Japanese Patent Application Nos. 2004-70976, filed Mar. 12, 2004; 2004-235553, filed Aug. 12, 2004; and 2004-367994, filed Dec. 20, 2004. The present invention relates to novel benzenedicarboxamides, processes for the preparation thereof, their intermediates and their use as insecticides. It was already known that phthalamide derivatives are useful as insecticides [see JP-A 11-240857 (1999), JP-A 2001-64258, JP-A 2001-64269, JP-A 2001-131141, JP-A 2003-40864, WO 01/21576 and WO 03/11028], and also that they show medicinal function [see JP-A 59-163353 (1984)]. There have now been found novel benzenedicarboxamides of the formula (I) wherein X represents hydrogen, halogen atom, nitro, C 1-6 alkylsulfonyloxy, C 1-6 alkylsulfinyl, C 1-6 alkylsulfenyl or C 1-6 alkylsulfonyl,R 1 represents C 1-6 alkyl, C 1-6 alkylthio-C 1-6 alkyl, C 1-6 alkylsulfinyl-C 1-6 alkyl or C 1-6 alkylsulfonyl-C 1-6 alkyl,Y represents halogen or C 1-6 alkyl,m represents 0 or 1,A represents O, S, SO, SO 2 , CH 2 or CH(CH 3 ), andQ represents a 5- or 6-membered heterocyclic group that contains at least one hetero atom selected from the group consisting of N, O and S and can be optionally substituted. The compounds of the formula (I), according to the invention, can be obtained by (a) reacting compounds of the formula (II) wherein R 1 and X have the same definitions as aforementioned,with compounds of the formula (III) wherein Y, A, m and Q have the same definitions as aforementioned,in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or(b) reacting compounds of the formula (IV) wherein X, Y, A, m and Q have the same definitions as aforementioned,with compounds of the formula (V) H 2 N—R 1 (V)wherein R 1 has the same definitions as aforementioned,in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or(c) reacting compounds of the formula (VI) wherein X and R 1 have the same definitions as aforementioned,with the compounds of the formula (III), wherein Y, A, m and Q have the same definitions as aforementioned,in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or(d) reacting compounds of the formula (VII) wherein X, Y, A, m and Q have the same definitions as aforementioned,with the compounds of the formula (V), H 2 N—R 1 (V)wherein R 1 has the same definitions as aforementioned,in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or(e) compounds of the formula (VIII) wherein X, Y, A, m and Q have the same definitions as aforementioned,are reacted with the compounds of the formula (V), H 2 N—R 1 (V)wherein R 1 has the same definitions as aforementioned,in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or(f) in the case that R 1 represents C 1-6 alkylsulfinyl-C 1-6 alkyl or C 1-6 alkylsulfonyl-C 1-6 alkyl in the formula (I), reacting compounds of the formula (If) whereinR 1f represents C 1-6 alkylthio-C 1-6 alkyl, andX, Y, A, m and Q have the same definitions as aforementioned,with an oxidizing agent in the presence of inert solvents. According to the present invention, the benzenedicarboxamides of the formula (I) show a strong insecticidal action. The compounds of the formula (I) are conceptually embraced in the general formula described in the aforementioned JP-A 11-240857 (1999). But they are not specifically disclosed at all in it and new compounds. Surprisingly, they show particularly remarkable insecticidal action compared with similar compounds described in the known prior art. In the present specification: “Halogen” represents fluorine, chlorine, bromine and iodine, and preferably represents fluorine, chlorine and bromine. “Alkyl” represents straight chain or branched chain C 1-12 alkyl, for example, methyl, ethyl, n- or iso-propyl, n-, iso-, sec- or tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, etc. and preferably represents C 1-6 alkyl. As each alkyl part in “alkylsulfonyloxy”, “alkylsulfenyl”, “alkylthioalkyl”, “alkylsulfinylalkyl”, “alkylsulfonylalkyl”, “alkoxy”, “alkylthio”, “alkylsulfinyl”, “alkylsulfonyl”, “haloalkyl”, “haloalkoxy”, “haloalkylthio”, “haloalkylsulfinyl”, “haloalkylsulfonyl” and “haloalkylcarbonyl”, there can be mentioned the same as described in the above-mentioned “alkyl” as examples. As each halogen part in “haloalkyl”, “haloalkoxy”, “haloalkylthio”, “haloalkylsulfinyl”, “haloalkylsulfonyl” and “haloalkylcarbonyl”, there can be mentioned the same as described in the above-mentioned “halogen” as examples. “5- or 6-membered heterocyclic group” contains at least one hetero atom selected from the group consisting of N, O and S, and preferably represents a heterocyclic group containing “one to three N atoms”, or “one O atom”, or “one S atom”, or “both one S atom and one to two N atoms”, or “both one O atom and one to two N atoms”, and as specific examples thereof, pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, furyl, thienyl, oxadiazolyl and pyrimidinyl, and moreover as most preferable examples thereof, pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, oxadiazolyl and pyrimidinyl are exemplified. In the compounds of the formula (I), according to the invention, the compounds in case that X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, C 1-4 alkylsulfonyloxy, C 1-4 alkylsulfinyl, C 1-4 alkylsulfenyl or C 1-4 alkylsulfonyl,R 1 represents C 1-4 alkyl, C 1-4 alkylthio-C 1-4 alkyl, C 1-4 alkylsulfinyl-C 1-4 alkyl or C 1-4 alkylsulfonyl-C 1-4 alkyl,Y represents fluorine, chlorine, bromine or C 1-4 alkyl,m represents 0 or 1,A represents O, S, SO, SO 2 , CH 2 or CH(CH 3 ), andQ represents 5-membered or 6-membered heterocyclic group that contains at least one hetero atom selected from a group consisting of N, O and S and can be optionally substituted by at least one selected from a group consisting of C 1-6 alkyl, C 1-6 alkoxy, C 1-6 alkylthio, C 1-6 alkylsulfinyl, C 1-6 alkylsulfonyl, C 1-10 haloalkyl, C 1-6 haloalkoxy, C 1-6 haloalkylthio, C 1-6 haloalkylsulfinyl, C 1-6 haloalkylsulfonyl, C 1-6 haloalkylcarbonyl, halogen, oxo and hydroxy group, can be mentioned as preferable. Above all, in the compounds of the formula (I), the compounds in case that X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, methanesulfonyloxy, C 1-2 alkylsulfinyl, C 1-2 alkylsulfenyl or C 1-2 alkylsulfonyl,R 1 represents isopropyl, C 1-2 alkylthio-C 3-4 alkyl, C 1-2 alkylsulfinyl-C 3-4 alkyl or C 1-2 alkylsulfonyl-C 3-4 alkyl,Y represents fluorine, chlorine or methyl,m represents 0 or 1,A represents O, S, SO, SO 2 , CH 2 or CH(CH 3 ), andQ represents heterocyclic group, selected from a group consisting of pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, oxadiazolyl and pyrimidinyl, that can be optionally substituted by at least one selected from the group consisting of C 1-4 alkyl, C 1-4 alkoxy, C 1-4 alkylthio, C 1-4 alkylsulfinyl, C 1-4 alkylsulfonyl, C 1-8 haloalkyl, C 1-4 haloalkoxy, C 1-4 haloalkylthio, C 1-4 haloalkylsulfinyl, C 1-4 haloalkylsulfonyl, C 1-4 haloalkylcarbonyl, fluorine, chlorine, bromine, iodine, oxo and hydroxy group, are particularly preferable. The compounds of the formula (I), according to the present invention, include stereo isomers (R/S configuration) in case that the group R 1 has an asymmetric carbon. The aforementioned process (a) can be illustrated by the following reaction scheme in case that, for example, 3-(1,1-dimethyl-2-methylthioethylimino)-4-iodo-3H-isobenzofuran-1-one and 1-(4-amino-3-methylbenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole are used as starting materials. The aforementioned preparation process (b) can be illustrated by the following reaction scheme in case that, for example, 2-{4-[3,5-bis(trifluoromethyl)pyrazole-1-ylmethyl]-2-methylphenyl}-4-fluoroisoindole-1,3-dione and (S)-1-methyl-2-methylthioethylamine are used as starting materials. The aforementioned preparation process (c) can be illustrated by the following reaction scheme in case that, for example, 3-iodo-N-(1,1-dimethyl-2-methylthioethyl)-phthalamic acid and 2-methyl-4-[1-(3-trifluoromethylpyrazole-1-yl)-ethyl]-aniline are used as starting materials. The aforementioned preparation process (d) can be illustrated by the following reaction scheme in case that, for example, 1-[4-(4-iodo-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(trifluoromethyl)-(1,2,4)-triazol and 1-methyl-2-methylthioethylamine are used as starting materials. The aforementioned preparation process (e) can be illustrated by the following reaction scheme in case that, for example, N-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methyl-phenyl}-6-iodo-phthalamic acid and 1-methyl-2-methylthioethylamine are used as starting materials. The aforementioned process (f) can be illustrated by the following reaction scheme in case that, for example, N 2 -(1-methyl-2-methylthioethyl)-3-iodo-N 1 -{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]phenyl}phthalamide and m-chloroperbenzoic acid are used as starting materials. The compounds of the formula (II), used as starting materials in the above-mentioned preparation process (a), are per se known compounds and can be easily prepared according to the process described in, for example, JP-A 11-240857 (1999), JP-A 2001-131141. As specific examples of the compounds of the formula (II), used as starting materials in the preparation process (a), there can be mentioned the following: 3-isopropylimino-3H-isobenzofuran-1-one,4-fluoro-3-isopropylimino-3H-isobenzofuran-1-one,4-chloro-3-isopropylimino-3H-isobenzofuran-1-one,4-bromo-3-isopropylimino-3H-isobenzofuran-1-one,4-iodo-3-isopropylimino-3H-isobenzofuran-1-one,3-(1-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,4-fluoro-3-(1-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,4-chloro-3-(1-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,4-bromo-3-(1-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,4-iodo-3-(1-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-4-fluoro-3H-isobenzofuran-1-one,4-chloro-3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,4-bromo-3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-1-one,3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-1-one,3-isopropylimino-1-oxo-1,3-dihydro-isobenzofuran-4-yl methanesulfonate3-(1-methyl-2-methylsulfanyl-ethylimino)-1-oxo-1,3-dihydro-isobenzofuran-4-yl methanesulfonate3-(1,1-dimethyl-2-methylsulfanyl-ethylimino)-1-oxo-1,3-dihydro-isobenzofuran-4-yl methanesulfonate and so on. The compounds of the formula (III), used as starting materials in the above-mentioned preparation process (a), which are partly novel compounds that are not described in the existing literature yet, can be obtained, for example, by reducing compounds of the formula (IX) wherein Y, A, m and Q have the same definitions as aforementioned, according to the catalytic hydrogen reduction process, a well-known process in the field of organic chemistry, with hydrogen in the presence of a catalytic reduction catalyst, for example, palladium carbon, Raney nickel, platinum oxide, etc. The above-mentioned catalytic hydrogen reduction process can be conducted in an adequate diluent. As examples of the diluent used in that case there can be mentioned ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, tetrahydrofuran (THF), etc.; alcohols, for example, methanol, ethanol, isopropanol, butanol, ethylene glycol, etc. and as catalytic reduction catalyst there can be mentioned, palladium carbon, Raney nickel, platinum oxide, etc. The reaction can be conducted at the temperatures generally from about 0 to about 100° C., preferably from room temperature (20° C.) to about 80° C. Said reaction can be conducted usually under normal pressure but can be operated optionally also under elevated pressure. For example, a compound of the formula (III) can be obtained by hydrogenating the compounds of the formula (IX) in a diluent, for example, ethanol, in the presence of 0.1-10% (w/w) palladium carbon. Also by a reduction reaction using metals etc. instead of catalytic hydrogen reduction, the compounds of the formula (III) can be obtained from the compounds of the formula (IX). As a reduction process using metals etc., there can be mentioned, for example, a process of reacting iron powder in acetic acid, a process of reacting zinc dust under neutral condition (Organic Syntheses Collective Vol. II, p. 447), a process of reacting stannic chloride under acidic condition (Organic Syntheses Collective Vol. II, p. 254), a process of reacting titanium trichloride under neutral condition, etc. The compounds of the formula (IX) are novel compounds and can be obtained by reacting the compounds of the formula (IX) wherein A represents other than oxygen atom, for example, compounds of the formula (X) wherein Y and m have the same definitions as aforementioned, A 1 represents S, SO, SO 2 , CH 2 or CH(CH 3 ), and M represents chlorine, bromine or methanesulfonyloxy, with compounds of the formula (XI) H-Q (XI) wherein Q has the same definition as aforementioned. The compounds of the formula (X), are well known in the field of organic chemistry and described in publications, for example, Chem. Abstr., Vol. 58, 3444e (1963); Bull. Soc. Chim. Fr. (1934), p. 539-545; J. Chem. Res. Miniprint, Vol. 8 (1987), p. 2133-2139; J. Chem. Soc. B (1967), p. 1154-1158; J. Chem. Soc. (1961), p. 221-222; J. Amer. Chem. Soc., Vol. 111 (1989), p. 5880-5886; J. Amer. Chem. Soc., Vol. 96 (1974), p. 7770-7781; Can. J. Chem., Vol. 68 (1990), p. 1450-1455, Tetrahedron Letter, vol. 35 (1994), p. 7391-7394. As specific examples of the compounds of the formula (X), there can be mentioned specifically 2-methyl-4-nitrobenzyl chloride,3-methyl-4-nitrobenzyl chloride4-nitrobenzyl methanesulfonate2-methyl-4-nitrobenzyl methanesulfonate3-methyl-4-nitrobenzyl methanesulfonate,4-nitrobenzenesulfenyl chloride,4-nitrobenzenesulfinyl chloride,4-nitrobenzenesulfonyl chloride,4-nitro-3-methylbenzenesulfonyl chloride,3-fluoro-4-nitrobenzyl bromide,3-chloro-4-nitrobenzyl chloride and so on. The nitro-substituted benzoic acids and their esters, starting materials of the compounds of the formula (X), are known compounds described in, for example, Chem. Ber., Vol. 52 (1919), p. 1083; Bull. Soc. Chim. Fr. (1962), p. 2255-2261; Tetrahedron (1985), p. 115-118; Chem. Pharm. Bull., Vol. 41 (1993), p. 894-906; WO 2001/042227. The compounds of the formula (XI) include known compounds and as their specific examples, there can be mentioned: 3,5-bis(trifluoromethyl)-1H-pyrazole,5-difluoromethoxy-3-trifluoromethyl-1H-pyrazole,4-pentafluoroethyl-1H-pyrazole,5-hexafluoro-n-propyl-1H-pyrazole,3,5-bis(trifluoromethyl)-1H-(1,2,4)-triazole,5-pentafluoroethyl-3-trifluoromethyl-1H-(1,2,4)-triazole,5-difluoromethyl-3-trifluoromethyl-1H-(1,2,4)-triazole,5-hydroxy-3,5-bis(trifluoromethyl)-1H-4,5-dihydropyrazole,2,4-bis(trifluoromethyl)-1H-imidazole,3-(2,2,2-trifluoroethyl)-5-trifluoromethyl-1,2-dihydro-(1,3,4)-triazol-2-one,2,5-bis(trifluoromethyl)-(1,3,4)-triazole,5-pentafluoroethyl-1H-pyrazole,3-pentafluoroethyl-1H-pyrazole,4-bromo-3-trifluoromethyl-1H-pyrazole,3-trifluoromethyl-1H-pyrazole,5-(difluoromethyl)-1,2-dihydro-2-methyl-3H-(1,2,4)-triazol-3-one,4-(trifluoromethyl)-2H-1,2,3-triazole,4-iodo-3-pentafluoroethyl-1H-pyrazole,3-pentafluoroethyl-4-(1,1,2,2-tetrafluoroethyl)-1H-pyrazole,3,4-bis-pentafluoroethyl-1H-pyrazole,3,5-diiodo-4-methyl-1H-pyrazole,3-Heptafluoropropylsulfanyl-5-trifluoromethyl-1H-(1,2,4)-triazole,3,5-bis(pentafluoroethyl)-1H-(1,2,4)-triazole and so on. The above-mentioned reaction of the compounds of the formula (X) with the compounds of the formula (XI) can be conducted in an adequate diluent. As examples of the diluent used in that case there can be mentioned, for example, aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; ketones, for example, acetone, methyl ethyl ketone (MEK), methyl isopropyl ketone, methyl isobutyl ketone (MIBK), etc.; nitriles, for example, acetonitrile, propionitrile, acrylonitrile, etc.; esters, for example, ethyl acetate, amyl acetate, etc.; acid amides, for example, dimethylformamide (DMF), dimethylacetamide (DMA), N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, hexamethyl phosphoric triamide (HMPA), etc. The reaction can be conducted in the presence of an acid binder and as said acid binder there can be mentioned, for example, as inorganic base, hydrides, hydroxides, carbonates, bicarbonates, etc. of alkali metals or alkaline earth metals, for example, sodium hydride, lithium hydride, sodium hydrogen carbonate, potassium hydrogen carbonate, sodium carbonate, potassium carbonate, lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, etc.; inorganic alkali metal amides, for example, lithium amide, sodium amide, potassium amide, etc.; as organic base, alcoholates, tertiary amines, dialkylaminoanilines and pyridines, for example, triethylamine, 1,1,4,4-tetramethylethylenediamine (TMEDA), N,N-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), 1,4-diazabicyclo[2,2,2]octane (DABCO), 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU), etc. The above-mentioned reaction can also be conducted by a process using a phase transfer catalyst in the presence of a diluent. As examples of the diluent used in that case there can be mentioned water; aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc. As examples of the phase transfer catalyst, quaternary ions, for example, tetramethylammonium bromide, tetrapropylammonium bromide, tetrabutylammonium bromide, tetrabutylammonium bissulfate, tetrabutylammonium iodide, trioctylmethylammonium chloride, benzyltriethylammonium bromide, butylpyridinium bromide, heptylpyridinium bromide, benzyltriethylammonium chloride, etc.; crown ethers, for example, dibenzo-18-crown-6, dicyclohexyl-18-crown-6, 18-crown-6, etc.; cryptands, for example, [2.2.2]-cryptate, [2.1.1]-cryptate, [2.2.1]-cryptate, [2.2.B]-cryptate, [3.2.2]-cryptate, etc. The above-mentioned reaction can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about 0 to about 200° C., preferably from room temperature (20° C.) to about 150° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the above-mentioned reaction, the aimed compounds of the formula (IX) can be obtained, for example, by reacting 1 mole to a little excess mole amount of the compounds of the formula (XI) to 1 mole of the compounds of the formula (X) in a diluent, for example, DMF, in the presence of potassium carbonate. As the compounds of the formula (IX) obtained according to the above-mentioned process, there can be mentioned, for example, the corresponding 4-nitrobenzyl derivatives to the 4-aminobenzyl derivatives of the formula (III) mentioned hereinafter. And, as one typical example, 1-(3-methyl-4-nitrobenzyl)-3,5-bis-(trifluoromethyl)-1H-pyrazole can be mentioned. Furthermore, in a case where Q represents 2-thiazolyl in the formula (IX), as a specific example, 2-(3-methyl-4-nitrobenzyl)-4-pentafluoroethyl-thiazole can be prepared by the following way in which a known compound, 3-methyl-4-nitrobenzylcyanide (see J. Chem. Soc., vol. 97 (1910), p. 2260) is reacted with hydrogen sulfide, and then the product, 3-methyl-4-nitro-benzylthioamide is reacted with a commercial product, 1-bromo-3,3,4,4,4-pentafluoro-2-butanone and then cyclized, according to a method described in J. Heterocycl. Chem., vol. 28 (1991) p. 907 to 911. In a case where Q represents 1,3,4-oxadiazol-2-yl in the formula (IX), as a specific example, 2-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-1,3,4-oxazole can easily be obtained, according to a method described in Heterocycles, (1994), vol. 38, p. 981 to 990, from the corresponding aldoxime as a starting material which can be prepared by a method described in Justus Liebigs Ann. Chem., (1927) vol. 45, p. 166. And, as another specific example, 2-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-1,3,4-oxazole can easily be obtained, according to a method described in Heterocycles, (1994) vol. 38, p. 981 to 990, from the corresponding 3-methyl-4-nitrobenzaldehyde oxime. In the above preparation, the oxime can be obtained from a known 3-methyl-4-nitrobenzaldehyde [see J. Chem. Soc. B, (1967) p. 1154 to 1158] as a starting material, according to methods described in J. Chem. Soc. C, (1969) p. 986 to 990 and then Tetrahedron Letter, vol. 35 (1994) p. 9099 to 9100. In a case where Q represents 2H-1,2,3-triazol-2-yl in the formula (IX), as a specific example, 2-(3-methyl-4-nitrobenzyl)-2H-4-trifluoromethyl-1,2,3-triazole can easily be prepared by a reaction of a known 3-methyl-4-nitrobenzyl chloride with a known 2H-4-trifluoromethyl-1,2,3-triazole described in J. Chem. Soc., Perkin Transaction 2, vol. 10 (1989) p. 1355 to 1375. In a case where Q represents 1H-1,2,4-triazol-1-yl in the formula (IX), as a specific example, 5-(3-methyl-4-nitrophenylsulfanyl)-1-methyl-3-trifluoromethyl-1H-1,2,4-triazole can easily be prepared by a reaction of 1-fluoro-3-methyl-4-nitrobenzene with a known 5-mercapto-1-methyl-3-trifluoromethyl-1H-1,2,4-triazole described in J. Med. Chem., vol. 35 (1992) p. 2103 to 2112, according to the same preparation as Synthesis Example 47 hereinafter. In a case where Q represents 1,2,4-oxazol-3-yl in the formula (IX), as a specific example, 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-1,2,4-oxazole can easily be obtained from 3-methyl-4-nitrobenzamideoxime, according to a method described in J. Org. Chem., vol. 68(2), 2003, p. 605-608. And, 3-methyl-4-nitrobenzamideoxime can be prepared by a reaction of a commercial 3-methyl-4-nitrobenzonitrile with hydroxylamine, according to a method described in Chem. Ber., vol. 22 (1889), p. 2428. And, as another specific example, 3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-1,2,4-oxazole can easily be obtained from 2-(3-methyl-4-nitrophenyl)-acetamideoxime as well, according to a method described in J. Org. Chem., vol. 68(2), 2003, p. 605-608. And, 2-(3-methyl-4-nitrophenyl)acetamideoxime can be prepared by a reaction of 3-methyl-4-nitrophenyl-acetonitrile with hydroxylamine, according to a method described in Chem. Ber., vol. 22 (1889), p. 2428. In a case where Q represents 1H-1,2,4-triazol-3-yl in the formula (IX), as specific examples, 1-methyl-3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-1H-1,2,4-triazole can easily be prepared by a reaction of the above 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-1,2,4-oxazole with methylhydrazine, according to a method described in J. Org. Chem., vol. 68(2), 2003, p. 605-608, and also 1-methyl-3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-1H-1,2,4-triazole can be done by a reaction of the above 3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-1,2,4-oxazole with methylhydrazine as well. The compounds of the formula (IX) can be prepared, besides the above-mentioned preparation process, also by the process to be mentioned later in Examples as an alternative. As specific examples of the compounds of the formula (III) there can be mentioned, for example, the following: 1-(4-amino-3-methylbenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole,1-(4-amino-3-methylbenzyl)-5-difluoromethoxy-3-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylbenzyl)-4-pentafluoroethyl-1H-pyrazole,1-(4-amino-3-methylbenzyl)-5-hexafluoro-n-propyl-1H-pyrazole,1-(4-amino-3-methylbenzyl)-3,5-bis(trifluoromethyl)-1H-(1,2,4)-triazole,1-(4-amino-3-methylbenzyl)-5-pentafluoroethyl-3-trifluoromethyl-1H-(1,2,4)-triazole,1-(4-amino-3-methylbenzyl)-5-difluoromethyl-3-trifluoromethyl-1H-(1,2,4)-triazole,4-(4-amino-3-methylbenzyl)-5-difluoromethoxy-1-difluoromethyl-3-trifluoromethyl-1H-pyrazole,4-(4-amino-3-methylbenzyl)-3-difluoromethoxy-1-difluoromethyl-5-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylbenzyl)-5-hydroxy-3,5-bis(trifluoromethyl)-1H-4,5-dihydropyrazole,1-(4-amino-3-methylbenzyl)-2,4-bis(trifluoromethyl)-1H-imidazole,4-(4-amino-3-methylbenzyl)-2-(2,2,2-trifluoroethyl)-5-trifluoromethyl-2,4-dihydro-3H-(1,2,4)-triazol-3-one,2-(4-amino-3-methylbenzyl)-4-(2,2,2-trifluoroethyl)-5-trifluoromethyl-2,4-dihydro-3H-(1,2,4)-triazol-3-one,1-(4-amino-3-methylbenzyl)-2,5-bis(trifluoromethyl)-1,3,4-triazole,2-(4-amino-3-methylbenzyl)-4,6-bis(trifluoromethyl)-pyrimidine,2-(4-amino-3-methylphenoxy)-4,6-bis(trifluoromethyl)-pyrimidine,1-(4-amino-3-methylphenyl)-3,5-bis(trifluoromethyl)-1H-pyrazole,1-(4-amino-3-methylphenyl)-5-pentafluoroethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-3-pentafluoroethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-4-pentafluoroethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-3-methyl-5-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-5-methyl-3-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-3-pentafluoroethyl-5-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-4-bromo-3-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-3-trifluoromethyl-1H-pyrazole,1-(4-amino-3-methylphenyl)-5-hydroxy-3-(2,2,2-trifluoroethyl)-5-trifluoromethyl-1H-4,5-dihydropyrazole,5-(4-amino-3-methylphenyl)-1-(2,2,2-trifluoroethyl)-3-trifluoromethyl-pyrazole,5-(4-amino-3-methylphenyl)-1-difluoromethyl-3-trifluoromethyl-pyrazole,3-(4-amino-3-methylphenyl)-1-difluoromethyl-3-difluoromethoxy-pyrazole,1-(4-amino-3-methylbenzyl)-3,4-bis(pentafluoroethyl)-1H-pyrazole,1-(4-amino-3-methylbenzyl)-3,5-bis(pentafluoroethyl)-1H-pyrazole,1-(4-amino-3-methylbenzyl)-3,4-bis(pentafluoropropyl)-1H-pyrazole,1-(4-amino-3-methylbenzyl)-3,5-bis(pentafluoropropyl)-1H-pyrazole,1-(4-amino-3-methylbenzyl)-3,5-bis(pentafluoroethyl)-1H-(1,2,4)-triazole,1-(4-amino-3-methylbenzyl)-2,5-bis(pentafluoroethyl)-1H-(1,3,4)-triazole,2-(4-amino-3-methylphenyl)-5-(trifluoromethyl)-1,3,4-oxadiazole,2-(4-amino-3-methylphenyl)-5-(pentafluoroethyl)-1,3,4-oxadiazole,2-(4-amino-3-methylphenyl)-5-(heptafluoropropyl)-1,3,4-oxadiazole,2-(4-amino-3-methylbenzyl)-5-(trifluoromethyl)-1,3,4-oxadiazole,2-(4-amino-3-methylbenzyl)-4-(trifluoromethyl)-2H-1,2,3-triazole,2-(4-amino-3-methylbenzyl)-4-(pentafluoroethyl)-thiazole,5-(4-amino-3-methylphenyl)sulfanyl-1-methyl-3-(trifluoromethyl)-1H-1,2,4-triazole,3-(4-amino-3-methylphenyl)-5-(trifluoromethyl)-1,2,4-oxadiazole,3-(4-amino-3-methylphenyl)-1-methyl-5-(trifluoromethyl)-1H-1,2,4-triazole,1-(4-amino-3-chlorobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole,1-(4-amino-3-fluorobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole and so on. The compounds of the formula (IV), used as starting materials in the above-mentioned preparation process (b), are novel compounds and can be easily obtained according to the process described in Japanese Laid-open Patent Publication No. 61-246161 (1986), for example, by reacting compounds of the formula (XII) wherein X has the same definition as aforementioned, with the compounds of the formula (III). wherein Y, A, m and Q have the same definitions as aforementioned, The reaction can be conducted in an adequate diluent. As the diluent used in that case there can be mentioned, for example, aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; esters, for example, ethyl acetate, amyl acetate, etc.; acid amides, for example, dimethylformamide (DMF), dimethylacetamide (DMA), N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, hexamethyl phosphoric triamide (HMPA), etc.; acids, for example, acetic acid etc. The reaction can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from room temperature (20° C.) to about 200° C., preferably from room temperature to 150° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the reaction, the aimed compounds of the formula (IV) can be obtained, for example, by reacting equimolar to a little excess mole amount of the compounds of the formula (III) to 1 mole of the compounds of the formula (XII) in a diluent, for example, acetic acid. Many of the compounds of the above-mentioned formula (XII) are publicly known, and as their specific examples there can be mentioned, phthalic anhydride, 3-fluorophthalic anhydride, 3-chlorophthalic anhydride, 3-bromophthalic anhydride, 3-iodophthalic anhydride, 3-methanesulfonyloxyphthalic anhydride, etc. Among the above-mentioned compounds, 3-methanesulfonyloxyphthalic anhydride can be easily obtained from 3-hydroxyphthalic anhydride and methanesulfonyl chloride according to the process described in Tetrahedron Letters Vol. 29, p. 5595-8 (1988). As specific examples of the compounds of the formula (IV), used as starting materials in the preparation process (b), there can be mentioned the following: 4-chloro-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]phenyl}-isoindole-1,3-dione,2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-difluoromethoxy-3-trifluoromethyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-bromo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-bromo-2-[2-methyl-4-(5-difluoromethoxy-3-trifluoromethyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-bromo-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-difluoromethoxy-3-trifluoromethyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl-methyl)-phenyl-]isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-hexafluoro-n-propyl-1H-pyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-methanesulfonyloxy-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[5-pentafluoroethyl-3-trifluoromethyl-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl} isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[5-difluoromethoxy-1-difluoromethyl-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[5-pentafluoroethyl-3-trifluoromethyl-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[5-difluoromethyl-3-trifluoromethyl-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-methanesulfonyloxy-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-(1,2,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-difluoromethoxy-1-difluoromethyl-3-trifluoromethyl-1H-pyrazol-4-yl-methyl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-hydroxy-3,5-bis(trifluoromethyl)-1H-4,5-dihydropyrazol-1-yl-methyl)-phenyl]-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[2,4-bis(trifluoromethyl)-1H-imidazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[3-(2,2,2-trifluoroethyl)-5-trifluoromethyl-1,2-dihydro-(1,3,4)-triazol-2-on-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[4-(2,2,2-trifluoroethyl)-3-trifluoromethyl-4,5-dihydro-(1,2,4)-triazol-5-on-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[2,5-bis(trifluoromethyl)-(1,3,4)-triazol-1-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[4,6-bis(trifluoromethyl)pyrimidin-2-yl-methyl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[4,6-bis(trifluoromethyl)pyrimidin-2-yloxy]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]-phenyl}-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(3-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-[3-methyl-5-trifluoromethyl-1H-pyrazol-1-yl]-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-methyl-3-trifluoromethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(3-pentafluoroethyl-5-trifluoromethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(4-bromo-3-trifluoromethyl-1H-pyrazol-1-yl)phenyl]isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(3-trifluoromethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[5-hydroxy-3-(2,2,2-trifluoroethyl)-5-trifluoromethyl-1H-4,5-dihydropyrazol-1-yl]-phenyl}-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[1-(2,2,2-trifluoroethyl)-3-trifluoromethyl-pyrazol-5-yl]-phenyl}-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(1-difluoromethyl-3-trifluoromethyl-pyrazol-5-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(1-difluoromethyl-3-difluoromethoxy-pyrazol-3-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]-phenyl}-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(3-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-bromo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]-phenyl}-isoindole-1,3-dione,4-bromo-2-[2-methyl-4-(5-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl-isoindole-1,3-dione,4-bromo-2-[2-methyl-4-(3-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-bromo-2-[2-methyl-4-(4-pentafluoroethyl-1H-pyrazol-1-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,4-bis(pentafluoroethyl)-1H-pyrazol-1-ylmethyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,5-bis(pentafluoroethyl)-1H-pyrazol-1-ylmethyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,4-bis(heptafluoropropyl)-1H-pyrazol-1-ylmethyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[3,5-bis(heptafluoropropyl)-1H-pyrazol-1-ylmethyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-pentafluoroethyl-1,3,4-oxadiazol-2-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-heptafluoropropyl-1,3,4-oxadiazol-2-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl-methyl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(4-trifluoromethyl-2H-1,2,3-triazol-2-yl-methyl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(4-(pentafluoroethyl)-thiazol-2-yl-methyl)-phenyl]-isoindole-1,3-dione,4-chloro-2-{2-methyl-4-[1-methyl-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl-sulfanyl]-phenyl}-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-phenyl]-isoindole-1,3-dione,4-chloro-2-[2-methyl-4-(1-methyl-5-trifluoromethyl-1H-1,2,4-triazol-3-yl)-phenyl]-isoindole-1,3-dione,4-iodo-2-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl)-phenyl]-isoindole-1,3-dione and so on. The compounds of the formula (V), used as starting materials in the preparation process (b), are either compounds well known in the field of organic chemistry or can be synthesized according to the process described in DE-A 20 45 905, WO 01/23350. As their specific examples there can be mentioned ethylamine, diethylamine, n-propylamine, isopropylamine, n-butylamine, sec-butylamine, isobutylamine, t-butylamine, t-amylamine, 2-(methyl thio)-ethylamine, 2-(ethylthio)-ethylamine, 1-methyl-2-(methylthio)-ethylamine, 1,1-dimethyl-2-(methylthio)-ethylamine and so on. The compounds of the formula (VI), used as starting materials in the preparation process (c), include publicly known compounds and can be easily prepared according to the process described in JP-A 11-240857 (1999), JP-A 2001-131141, etc. As their specific examples there can be mentioned the following: N-isopropyl-phthalamic acid,3-fluoro-N-isopropyl-phthalamic acid,3-chloro-N-isopropyl-phthalamic acid,3-bromo-N-isopropyl-phthalamic acid,3-iodo-N-isopropyl-phthalamic acid,N-(1-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,3-fluoro-N-(1-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,3-chloro-N-(1-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,3-bromo-N-(1-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,3-iodo-N-(1-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid,N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-3-fluoro-phthalamic acid,3-chloro-N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid,3-bromo-N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid,N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-3-iodo-phthalamic acid,N-isopropyl-3-methanesulfonyloxy-phthalamic acid,N-(1-methyl-2-methylsulfanyl-ethyl)-3-methanesulfonyloxy-phthalamic acid,N-(1-methyl-2-methylsulfanyl-ethyl)-3-nitro-phthalamic acid,3-chloro-N-(2-ethylsulfanyl-1-methyl-ethyl)-phthalamic acid,3-bromo-N-(2-ethylsulfanyl-1-methyl-ethyl)-phthalamic acid,N-(2-ethylsulfanyl-1-methyl-ethyl)-3-iodo-phthalamic acid,N-(2-ethylsulfanyl-1-methyl-ethyl)-3-nitro-phthalamic acid,N-(2-ethylsulfanyl-1-methyl-ethyl)-3-methanesulfonyloxy-phthalamic acid,N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-3-methanesulfonyloxy-phthalamic acid and so on. The above-mentioned compounds of the formula (VI) can be easily obtained generally by reacting phthalic anhydrides of the aforementioned formula (XII) wherein X has the same definition as aforementioned, with amines of the formula H 2 N—R 1 (XIII) wherein R 1 has the same definitions as aforementioned, The compounds of the above-mentioned formula (II) are well known in the field of organic chemistry and there can be specifically mentioned, for example, ethylamine, n-propylamine, isopropylamine, n-butylamine, sec-butylamine, isobutylamine, t-butylamine, t-amylamine, 2-(methylthio)ethylamine, 2-(ethylthio)ethylamine, 1-methyl-2-(methylthio)ethylamine, 1,1-dimethyl-2-(methylthio)ethylamine, etc. These amines can be easily obtained also by the process described in DE-A 20 45 905, WO 01/23350, etc. The above-mentioned reaction of the compounds of the formula (XII) with the amines of the formula (XIII) can be conducted according to the process described in, for example, J. Org. Chem., Vol. 46, p. 175 (1981) etc. Said reaction can be conducted in an adequate diluent, and as examples of the diluent used in that case there can be mentioned aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether DGM), etc.; ketones, for example, acetone, methyl ethyl ketone (MEK), methyl isopropyl ketone, methyl isobutyl ketone (MIBK), etc.; nitriles, for example, acetonitrile, propionitrile, acrylonitrile, etc.; esters, for example, ethyl acetate, amyl acetate, etc. The above-mentioned reaction can be conducted in the presence of a base, and as said base there can be mentioned, for example, tertiary amines, dialkylaminoanilines and pyridines, for example, triethylamine, 1,1,4,4-tetramethylethylenediamine (TMEDA), N,N-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), 1,4-diazabicyclo[2,2,2]octane (DABCO), 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU), etc. The above-mentioned reaction can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about −70 to about 100° C., preferably from about −50 to about 80° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the above-mentioned reaction, the aimed compounds of the formula (VI) can be obtained, for example, by reacting 1-4 moles of the compounds of the formula (XIII) to 1 mole of the compounds of the formula (XII) in a diluent, for example, acetonitrile. The compounds of the formula (VII), used as starting materials in the preparation process (d), are novel compounds and can be easily obtained, for example, by reacting the compounds of the formula (VIII), starting materials in the below-mentioned preparation process (e), according to the process described in J. Med. Chem., Vol. 10, p. 982 (1967) etc. in the presence of a condensing agent. As specific examples of the compounds of the formula (VII), there can be mentioned the following: 1-[4-(4-iodo-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(trifluoromethyl)-1H-pyrazole,1-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(trifluoromethyl)-1H-pyrazole,1-[4-(4-iodo-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(trifluoromethyl)-1,2,4-triazole,1-[4-(4-iodo-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-3,5-bis(trifluoromethyl)-1H-pyrazole,1-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,4-bis(pentafluoroethyl)-1H-pyrazole,1-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(pentafluoroethyl)-1H-pyrazole,1-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,4-bis(heptafluoropropyl)-1H-pyrazole,1-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methyl-benzyl]-3,5-bis(heptafluoropropyl)-1H-pyrazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-5-(trifluoromethyl)-1,3,4-oxadiazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-5-(pentafluoroethyl)-1,3,4-oxadiazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-5-(heptafluoropropyl)-1,3,4-oxadiazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylbenzyl]-5-(trifluoromethyl)-1,3,4-oxadiazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylbenzyl]-4-(trifluoromethyl)-2H-1,2,3-triazole,2-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylbenzyl]-4-(pentafluoroethyl)thiazole,5-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]sulfanyl-1-methyl-3-(trifluoromethyl)-1H-1,2,4-triazole,3-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-5-(trifluoromethyl)-1,2,4-oxadiazole,3-[4-(4-chloro-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-1-methyl-5-(trifluoromethyl)-1H-1,2,4-triazole,2-[4-(4-iodo-3-oxo-3H-isobenzofuran-1-ylideneamino)-3-methylphenyl]-5-(trifluoromethyl)-1,3,4-oxadiazole and so on. The compounds of the formula (V), similarly used as starting materials in the preparation process (d), are the same as explained in the aforementioned preparation process (b). The compounds of the formula (VIII), used as starting materials in the preparation process (e), are novel compounds and can be easily obtained, for example, by reacting phthalic anhydrides of the aforementioned formula (XII) with the compounds of the aforementioned formula (III). The above-mentioned reaction can be conducted in an adequate diluent, and as examples of the diluent used in that case there can be mentioned aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; ketones, for example, acetone, methyl ethyl ketone (MEK), methyl isopropyl ketone, methyl isobutyl ketone (MIBK), etc.; nitriles, for example, acetonitrile, propionitrile, acrylonitrile, etc.; esters, for example, ethyl acetate, amyl acetate, etc. The above-mentioned reaction can be conducted in the presence of a base, and as said base there can be mentioned tertiary amines, dialkylaminoanilines and pyridines, for example, triethylamine, 1,1,4,4-tetramethylethylenediamine (TMEDA), N,N-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), 1,4-diazabicyclo[2,2,2]octane (DABCO) and 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU), etc. The above-mentioned reaction can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about −70 to about 100° C., preferably from about −50 to about 80° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. As specific examples of the compounds of the formula (VIII), there can be mentioned the following: N-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-2-methyl-phenyl}-6-iodo-phthalamic acid,N-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-2-methyl-phenyl}-6-chloro-phthalamic acid,N-{4-[3,5-bis(trifluoromethyl)-(1,2,4)-triazol-1-yl-methyl]-2-methyl-phenyl}-6-iodo-phthalamic acid,N-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]-2-methyl-phenyl}-6-iodo-phthalamic acid,N-{4-[3,4-bis(pentafluoroethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-6-chloro-phthalamic acid,N-{4-[3,5-bis(pentafluoroethyl)-1H-pyrazol-1-yl-methyl]-phenyl}-6-chloro-phthalamic acid,N-{4-[3,4-bis(heptafluoropropyl)-1H-pyrazol-1-yl-methyl]-phenyl}-6-chloro-phthalamic acid,N-{4-[3,5-bis(heptafluoropropyl)-1H-pyrazol-1-yl-methyl]-phenyl}-6-chloro-phthalamic acid,N-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(5-pentafluoroethyl-1,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(5-heptafluoropropyl-1,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl-methyl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(4-trifluoromethyl-2H-1,2,3-triazol-2-yl-methyl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(4-pentafluoroethyl-thiazol-2-yl-methyl)-phenyl]-6-chloro-phthalamic acid,N-{2-methyl-4-[1-methyl-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl-sulfanyl]-phenyl}-6-chloro-phthalamic acid,N-[2-methyl-4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(1-methyl-5-trifluoromethyl-1H-1,2,4-triazol-3-yl)-phenyl]-6-chloro-phthalamic acid,N-[2-methyl-4-(5-trifluoromethyl-1,3,4-oxadiazol-2-yl)-phenyl]-6-iodo-phthalamic acid and so on. The compounds of the formula (V), similarly used as starting materials in the preparation process (e), can be the same as ones used in the aforementioned preparation processes (b) and (d). The compounds of the formula (If), used as starting materials in the preparation process (f), are compounds included in the formula (I) of the present invention. By oxidizing the group R If in the compounds of the formula (If), namely, C 1-6 alkylthio-C 1-6 alkyl, the compounds of the formula (I), in which the group R If corresponds to C 1-6 alkylsulfinyl-C 1-6 alkyl or C 1-6 alkylsulfonyl-C 1-6 alkyl, can be obtained. The compounds of the formula (If) can be prepared by the processes of the aforementioned preparation processes (a), (b), (c), (d) and/or (e). As specific examples of the compounds of the formula (If), there can be mentioned the following: 3-iodo-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,N 2 -(1,1-dimethyl-2-methylsulfanyl-ethyl)-3-iodo-N 1 -{2-methyl-4-[3,5-bis(trifluoro-methyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,3-iodo-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,5-bis(trifluoromethyl)(1,2,4)-triazol-1-ylmethyl]-phenyl}phthalamide,3-chloro-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,3-chloro-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,4-bis(pentafluoro-ethyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,3-chloro-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,5-bis(pentafluoro-ethyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,3-chloro-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,4-bis(heptafluoro-propyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide,3-chloro-N 2 -(1-methyl-2-methylsulfanyl-ethyl)-N 1 -{2-methyl-4-[3,5-bis(heptafluoro-propyl)-1H-pyrazol-1-ylmethyl]-phenyl}phthalamide and so on The reaction of the aforementioned preparation process (a) can be conducted in an adequate diluent singly or mixed. As examples of the diluent used in that case there can be mentioned water; aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; nitriles, for example, acetonitrile, propionitrile, acrylonitrile, etc.; esters, for example, ethyl acetate, amyl acetate, etc. The preparation process (a) can be conducted in the presence of an acid catalyst, and as examples of said acid catalyst there can be mentioned mineral acids, for example, hydrochloric acid and sulfuric acid; organic acids, for example, acetic acid, trifluoroacetic acid, propionic acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, etc. The preparation process (a) can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about −20 to about 100° C., preferably from about 0 to about 100° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the preparation process (a), the aimed compounds of the formula (I) can be obtained, for example, by reacting 1 to a little excess mole amount of the compounds of the formula (III) to 1 mole of the compounds of the formula (II) in a diluent, for example, 1,2-dichloroethane in the presence of 0.01-0.1 mole amount of p-toluenesulfonic acid. The reaction of the aforementioned preparation process (b) can be conducted in an adequate diluent. As examples of the diluent used in that case there can be mentioned aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, pentane, hexane, cyclohexane, petroleum ether, ligroine, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; ethers, for example, ethyl ether, methyl ethyl ether, isopropyl ether, butyl ether, dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; esters, for example, ethyl acetate, amyl acetate, etc.; acid amides, for example, dimethylformamide (DMF), dimethylacetamide (DMA), N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, hexamethyl phosphoric triamide (HMPA), etc. The preparation process (b) can be conducted in the presence of an acid catalyst and as examples of said acid catalyst there can be mentioned mineral acids, for example, hydrochloric acid and sulfuric acid; organic acids, for example, acetic acid, trifluoroacetic acid, propionic acid, methanesulfonic acid, p-toluenesulfonic acid, etc. The preparation process (b) can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about −20 to about 150° C., preferably from room temperature (20° C.) to about 100° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the preparation process (b), the aimed compounds of the formula (I) can be obtained, for example, by reacting 1-25 moles of the compounds of the formula (V) to 1 mole of the compounds of the formula (IV) in a diluent, for example, dioxane in the presence of 0.01-0.5 mole amount of acetic acid. The aforementioned preparation processes (c), (d) and (e) can be conducted under the similar condition as the above-mentioned preparation process (a). The reaction of the aforementioned preparation process (f) can be conducted in an adequate diluent. As examples of the diluent used in that case there can be mentioned aliphatic, alicyclic and aromatic hydrocarbons (may be optionally chlorinated), for example, benzene, toluene, xylene, dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene, dichlorobenzene, etc.; alcohols, for example, methanol, ethanol, isopropanol and butanol; acids; formic acid, acetic acid, etc. As the oxidizing agents usable in the aforementioned preparation process (f) there can be mentioned, for example, m-chloroperbenzoic acid, peracetic acid, potassium metaperiodate, potassium hydrogen persulfate (oxon), hydrogen peroxide, etc. The preparation process (f) can be conducted in a substantially wide range of temperature. It is adequate to conduct it at the temperatures in a range of generally from about −50 to about 150° C., preferably from about −10 to about 100° C. Although said reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure. In conducting the preparation process (f), the aimed compounds of the corresponding formula (I) can be obtained, for example, by reacting 1-5 moles of an oxidizing agent to 1 mole of the compounds of the formula (If) in a diluent, for example, dichloromethane. The reaction of the aforementioned preparation process (f) can be conducted, for example, according to the process described in JIKKEN KAGAKU KOZA (Lecture on experimental chemistry) edited by the Chemical Society of Japan, 4 th , ed., Vol. 24, p. 350 (1992) published by MARUZEN or ibid. p. 365. The compounds of the formula (I) of the present invention show strong insecticidal action. The compounds of the formula (I), according to the present invention can, therefore, be used as insecticidal agents. And the active compounds of the formula (I) of the present invention exhibit exact controlling effect against harmful insects without giving phytotoxicity on cultured plants. And the compounds of the present invention can be used for controlling a wide variety of pests, for example, harmful sucking insects, biting insects and other plant-parasitic pests, stored grain pests, hygienic pests, etc. and applied for their extermination. As examples of such pests there can be mentioned the following pests: As insects, there can be mentioned: Coleoptera pests, for example, Callosobruchus Chinensis, Sitophilus zeamais, Tribolium castaneum, Epilachna vigintioctomaculata, Agriotes fuscicollis, Anomala rufocuprea, Leptinotarsa decemlineata, Diabrotica spp., Monochamus alternatus, Lissorhoptrus oryzophilus, Lyctus bruneus; Lepidoptera pests, for example, Lymantria dispar, Malacosoma neustria, Pieris rapae, Spodoptera litura, Mamestra brassicae, Chilo suppressalis, Pyrausta nubilalis, Ephestia cautella, Adoxophyes orana, Carpocapsa pomonella, Agrotis fucosa, Galleria mellonella, Plutella maculipennis, Heliothis virescens, Phyllocnistis citrella; Hemiptera pests, for example, Nephotettix cincticeps, Nilaparvata lugens, Pseudococcus comstocki, Unaspis yanonensis, Myzus persicae, Aphis pomi, Aphis gossypii, Rhopalosiphum pseudobrassicas, Stephanitis nashi, Nazara spp., Trialeurodes vaporariorum, Psylla spp.; Thysanoptera pests, for example, Thrips palmni, Frankliniella occidental; Orthoptera pests, for example, Blatella germanica, Periplaneta americana, Gryllotalpa africana, Locusta migratoria migratoriodes; Homoptera pests, for example, Reticulitermes speratus, Coptotermes formosanus; Diptera pests, for example, Musca domestica, Aedes aegypti, Hylemia platura, Culex pipiens, Anopheles slnensis, Culex tritaeniorhynchus, Liriomyzae trifolii etc. Moreover, as mites there can be mentioned, for example, Tetranychus cinnabarinus, Tetranychus urticae, Panonychus citri, Aculops pelekassi, Tarsonemus spp., etc. Furthermore, as nematodes there can be mentioned, for example, Meloidogyne incognita, Bursaphelenchus lignicolus Mamiya et Kiyohara, Aphelenchoides besseyi, Heterodera glycines, Pratylenchus spp., etc. In addition, in the field of veterinary medicine, the novel compounds of the present invention can be effectively used against various harmful animal-parasitic pests (endoparasites and ectoparasites), for example, insects and helminthes. As examples of such animal-parasitic pests there can be mentioned the following pests: As insects there can be mentioned, for example, Gastrophilus spp., Stomoxys spp., Trichodectes spp., Rhodnius spp., Ctenocephalides canis, Cimex lectularius etc. As mites there can be mentioned, for example, Ornithodoros spp., Ixodes spp., Boophilus spp., etc. In the present invention, substances having insecticidal action against pests, which include all of them, are in some cases called as insecticides. All plants and plant parts can be treated in accordance with the invention. Plants are to be understood as meaning in the present context all plants and plant populations such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional plant breeding and optimization methods or by biotechnological and genetic engineering methods or by combinations of these methods, including the transgenic plants and including the plant cultivars protectable or not protectable by plant breeders' rights. Plant parts are to be understood as meaning all parts and organs of plants above and below the ground, such as shoot, leaf, flower and root, examples which may be mentioned being leaves, needles, stalks, stems, flowers, fruit bodies, fruits, seeds, roots, tubers and rhizomes. The plant parts also include harvested material, and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds. Treatment according to the invention of the plants and plant parts with the active compounds is carried out directly or by allowing the compounds to act on the surroundings, environment or storage space by the customary treatment methods, for example by immersion, spraying, evaporation, fogging, scattering, painting on and, in the case of propagation material, in particular in the case of seeds, also by applying one or more coats. The active compounds, according to the present invention, can be converted into the customary formulation forms, when they are used as insecticides. As formulation forms there can be mentioned, for example, solutions, emulsions, wettable powders, water dispersible granules, suspensions, powders, foams, pastes, tablets, granules, aerosols, natural and synthetic materials impregnated with active compound, microcapsules, seed coating agents, formulations used with burning equipment (as burning equipment, for example, fumigation and smoking cartridges, cans, coils, etc.), ULV [cold mist, warm mist], etc. These formulations can be produced according to per se known methods, for example, by mixing the active compounds with extenders, namely liquid diluents or carriers; liquefied gas diluents or carriers; solid diluents or carriers, and optionally with surface-active agents, namely emulsifiers and/or dispersants and/or foam-forming agents. In case that water is used as extender, for example, organic solvents can also be used as auxiliary solvents. As liquid diluents or carriers there can be mentioned, for example, aromatic hydrocarbons (for example, xylene, toluene, alkylnaphthalene, etc.), chlorinated aromatic or chlorinated aliphatic hydrocarbons (for example, chlorobenzenes, ethylene chlorides, methylene chloride, etc.), aliphatic hydrocarbons [for example, cyclohexane etc. or paraffins (for example, mineral oil fractions etc.)], alcohols (for example, butanol, glycols and their ethers, esters, etc.), ketones (for example, acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, etc.), strongly polar solvents (for example, dimethylformamide, dimethyl sulfoxide, etc.), and water. Liquefied gas diluents or carriers are substances that are gases at normal temperature and pressure and there can be mentioned, for example, aerosol propellants such as butane, propane, nitrogen gas, carbon dioxide, halogenated hydrocarbons. As solid diluents there can be mentioned, for example, ground natural minerals (for example, kaolin, clay, talc, chalk quartz, attapulgite, montmorillonite, diatomaceous earth, etc.), ground synthetic minerals (for example, highly dispersed silicic acid, alumina, silicates, etc.). As solid carriers for granules there can be mentioned, for example, crushed and fractionated rocks (for example, calcite, marble, pumice, sepiolite, dolomite, etc.), synthetic granules of inorganic or organic meals, particles of organic materials (for example, saw dust, coconut shells, maize cobs, tobacco stalks, etc.), etc. As emulsifiers and/or foam-forming agents, there can be mentioned, for example, nonionic and anionic emulsifiers [for example, polyoxyethylene fatty acid esters, polyoxyethylene fatty acid alcohol ethers (for example, alkylaryl polyglycol ethers), alkylsulfonates, alkylsulfates, arylsulfonates, etc.], albumin hydrolysis products, etc. Dispersants include, for example, lignin sulfite waste liquor and methyl cellulose. Tackifiers can also be used in formulations (powders, granules, emulsifiable concentrates). As said tackifiers, there can be mentioned, for example, carboxymethyl cellulose, natural or synthetic polymers (for example, gum Arabic, polyvinyl alcohol, polyvinyl acetate, etc.). Colorants can also be used. As said colorants there can be mentioned, for example, inorganic pigments (for example, iron oxide, titanium oxide, Prussian Blue, etc.), organic dyestuffs such as alizarin dyestuffs, azo dyestuffs or metal phthalocyanine dyestuffs, and further trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc. Said formulations can contain the aforementioned active component of the amount in the range of generally 0.1-95% by weight, preferably 0.5-90% by weight. The active compounds of the formula (I) of the present invention can exist also as a mixed agent with other active compounds, for example, insecticides, poisonous baits, bactericides, miticides, nematicides, fungicides, growth regulators or herbicides in the form of their commercially useful formulations and in the application forms prepared from such formulations. Here, as the above-mentioned insecticides, there can be mentioned, for example, organophosphorous agents, carbamate agents, carboxylate type chemicals, chlorinated hydrocarbon type chemicals, insecticidal substances produced by microorganisms, etc. Further, the active compounds of the formula (I) of the present invention can exist also as a mixed agent with a synergist, and such formulations and application forms can be mentioned as commercially useful. Said synergist itself must not be active, but is a compound that enhances the action of the active compound. Particularly favourable mixing components are, for example, the following compounds: Fungicides: 2-phenylphenol; 8-hydroxyquinoline sulfate; acibenzolar-S-methyl; aldimorph; amidoflumet; ampropylfos; ampropylfos-potassium; andoprim; anilazine; azaconazole; azoxystrobin; benalaxyl; benalaxyl-M; benodanil; benomyl; benthiavalicarb-isopropyl; benzamacril; benzamacril-isobutyl; bilanafos; binapacryl; biphenyl; bitertanol; blasticidin-S; boscalid; bromuconazole; bupirimate; buthiobate; butylamine; calcium polysulfide; capsimycin; captafol; captan; carbendazim; carboxin; carpropamid; carvone; chinomethionat; chlobenthiazone; chlorfenazole; chloroneb; chlorothalonil; chlozolinate; clozylacon; cyazofamid; cyflufenamid; cymoxanil; cyproconazole; cyprodinil; cyprofuram; Dagger G; debacarb; dichlofluanid; dichlone; dichlorophen; diclocymet; diclomezine; dicloran; diethofencarb; difenoconazole; diflumetorim; dimethirimol; dimethomorph; dimoxystrobin; diniconazole; diniconazole-M; dinocap; diphenylamine; dipyrithione; ditalimfos; dithianon; dodine; drazoxolon; edifenphos; epoxiconazole; ethaboxam; ethirimol; etridiazole; famoxadone; fenamidone; fenapanil; fenarimol; fenbuconazole; fenfuram; fenhexamid; fenitropan; fenoxanil; fenpiclonil; fenpropidin; fenpropimorph; ferbam; fluazinam; flubenzimine; fludioxonil; flumetover; flumorph; fluoromide; fluoxastrobin; fluquinconazole; flurprimidol; flusilazole; flusulfamide; flutolanil; flutriafol; folpet; fosetyl-Al; fosetyl-sodium; fuberidazole; furalaxyl; furametpyr; furcarbanil; furmecyclox; guazatine; hexachlorobenzene; hexaconazole; hymexazol; imazalil; imibenconazole; iminoctadine triacetate; iminoctadine tris(albesilate); iodocarb; ipconazole; iprobenfos; iprodione; iprovalicarb; irumamycin; isoprothiolane; isovaledione; kasugamycin; kresoxim-methyl; mancozeb; maneb; meferimzone; mepanipyrim; mepronil; metalaxyl; metalaxyl-M; metconazole; methasulfocarb; methfuroxam; metiram; metominostrobin; metsulfovax; mildiomycin; myclobutanil; myclozolin; natamycin; nicobifen; nitrothal-isopropyl; noviflumuron; nuarimol; ofurace; orysastrobin; oxadixyl; oxolinic acid; oxpoconazole; oxycarboxin; oxyfenthiin; paclobutrazol; pefurazoate; penconazole; pencycuron; phosdiphen; phthalide; picoxystrobin; piperalin; polyoxins; polyoxorim; probenazole; prochloraz; procymidone; propamocarb; propanosine-sodium; propiconazole; propineb; proquinazid; prothioconazole; pyraclostrobin; pyrazophos; pyrifenox; pyrimethanil; pyroquilon; pyroxyfur; pyrrolnitrine; quinconazole; quinoxyfen; quintozene; simeconazole; spiroxamine; sulfur; tebuconazole; tecloftalam; tecnazene; tetcyclacis; tetraconazole; thiabendazole; thicyofen; thifluzamide; thiophanate-methyl; thiram; tioxymid; tolclofos-methyl; tolylfluanid; triadimefon; triadimenol; triazbutil; triazoxide; tricyclamide; tricyclazole; tridemorph; trifloxystrobin; triflumizole; triforine; triticonazole; uniconazole; validamycin A; vinclozolin; zineb; ziram; zoxamide; (2S)—N-[2-[4-[[3-(4-chlorophenyl)-2-propynyl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)amino]-butanamide; 1-(1-naphthalenyl)-1H-pyrrol-2,5-dione; 2,3,5,6-tetrachloro-4-(methylsulfonyl)-pyridine; 2-amino-4-methyl-N-phenyl-5-thiazolecarboxamide; 2-chloro-N-(2,3-dihydro-1,1,3-trimethyl-1H-inden-4-yl)-3-pyridinecarboxamide; 3,4,5-trichloro-2,6-pyridinedicarbonitrile; actinovate; cis-1-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)-cycloheptanol; methyl 1-(2,3-dihydro-2,2-dimethyl-1H-inden-1-yl)-1H-imidazole-5-carboxylate; mono potassium carbonate; N-(6-methoxy-3-pyridinyl)-cyclopropanecarboxamide; N-butyl-8-(1,1-dimethylethyl)-1-oxaspiro[4,5]decan-3-amine; sodium tetrathiocarbonate; and copper salts and preparations, such as Bordeaux mixture; copper hydroxide; copper naphthenate; copper oxychloride; copper sulphate; cufraneb; copper oxide; mancopper; oxine-copper. Bactericides: bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furancarboxylic acid, oxytetracyclin, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations. Insecticides/Acaricides/Nematicides: 1. Acetylcholinesterase (AChE) inhibitors 1.1 Carbamates (e.g. alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, azamethiphos, bendiocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, cloethocarb, coumaphos, cyanofenphos, cyanophos, dimetilan, ethiofencarb, fenobucarb, fenothiocarb, formetanate, furathiocarb, isoprocarb, metam-sodium, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, promecarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC, xylylcarb) 1.2 Organophosphates (e.g. acephate, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothion, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos (-methyl/-ethyl), coumaphos, cyanofenphos, cyanophos, chlorfenvinphos, demeton-s-methyl, demeton-s-methylsulphon, dialifos, diazinon, dichlofenthion, dichlorvos/ddvp, dicrotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, epn, ethion, ethoprophos, etrimfos, famphur, fenamiphos, fenitrothion, fensulfothion, fenthion, flupyrazofos, fonofos, formothion, fosmethilan, fosthiazate, heptenophos, iodofenphos, iprobenfos, isazofos, isofenphos, isopropyl o-salicylate, isoxathion, malathion, mecarbam, methacrifos, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion (-methyl/-ethyl), phenthoate, phorate, phosalone, phosmet, phosphamidon, phosphocarb, phoxim, pirimiphos (-methyl/-ethyl), profenofos, propaphos, propetamphos, prothiofos, prothoate, pyraclofos, pyridaphenthion, pyridathion, quinalphos, sebufos, sulfotep, sulprofos, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, triclorfon, vamidothion) 2. Sodium channel modulators/voltage dependant sodium channel blockers 2.1 Pyrethroids (e.g. acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-s-cyclopentyl-isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin, cis-resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, DDT, deltamethrin, empenthrin (1R-isomer), esfenvalerate, etofenprox, fenfluthrin, fenpropathrin, fenpyrithrin, fenvalerate, flubrocythrinate, flucythrinate, flufenprox, flumethrin, fluvalinate, fubfenprox, gamma-cyhalothrin, imiprothrin, kadethrin, lambda-cyhalothrin, metofluthrin, permethrin (cis-, trans-), phenothrin (1R-trans isomer), prallethrin, profluthrin, protrifenbute, pyresmethrin, resmethrin, RU 15525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin, tetramethrin (1R-isomer), tralomethrin, transfluthrin, ZXI 8901, pyrethrins (pyrethrum)) 2.2 Oxadiazine (e.g. indoxacarb) 3. Acetylcholine receptor agonists/-antagonists 3.1 Chloronicotinyls/neonicotinoids (e.g. acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine, thiacloprid, thiamethoxam) 3.2 nicotine, bensultap, cartap 4. Acetylcholine receptor modulators 4.1 Spinosyns (e.g. spinosad) 5. GABA gated chloride channel antagonists 5.1 Cyclodiene organochlorines (e.g. camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor 5.2 Fiproles (e.g. acetoprole, ethiprole, fipronil, vaniliprole) 6. Chloride channel activators 6.1 Mectins (e.g. abamectin, avermectin, emamectin, emamectin-benzoate, ivermectin, milbemectin, milbemycin) 7. Juvenile hormone mimics (e.g. diofenolan, epofenonane, fenoxycarb, hydroprene, kinoprene, methoprene, pyriproxifen, triprene) 8. Ecdysone agonists/disruptors 8.1 Diacylhydrazines (e.g. chromafenozide, halofenozide, methoxyfenozide, tebufenozide) 9. Inhibitors of chitin biosynthesis 9.1 Benzoylureas (e.g. bistrifluron, chlofluazuron, diflubenzuron, fluazuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron) 9.2 buprofezin 9.3 cyromazine 10. Inhibitors of oxidative phosphorylation, ATP-disruptors 10.1 diafenthiuron 10.2 Organotins (e.g. azocyclotin, cyhexatin, fenbutatin-oxide) 11. Decoupler of oxidative phosphorylation by disruption of H proton gradient 11.1 Pyrroles (e.g. chlorfenapyr) 11.2 Dinitrophenoles (e.g. binapacyrl, dinobuton, dinocap, DNOC) 12. Site I electron transport inhibitors 12.1 METI's (e.g. fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad) 12.2 hydramethylnone 12.3 dicofol 13. Site II electron transport inhibitors 13.1 rotenone 14. Site III electron transport inhibitors 14.1 acequinocyl, fluacrypyrim 15. Microbial disruptors of insect midgut membranes Bacillus thuringiensis strains 16. Inhibitors of lipid synthesis 16.1 Tetronic acid insecticides (e.g. spirodiclofen, spiromesifen) 16.2 Tetramic acid insecticides [e.g. 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-yl ethyl carbonate (alias: carbonic acid, 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]-dec-3-en-4-yl ethyl ester, CAS-Reg.-No.: 382608-10-8) and carbonic acid, cis-3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-1-azaspiro[4.5]dec-3-en-4-yl ethyl ester (CAS-Reg.-No.: 203313-25-1)] 17. Carboxamides (e.g. flonicamid) 18. Octopaminergic agonists (e.g. amitraz) 19. Inhibitors of magnesium stimulated ATPase (e.g. propargite) 20. Phthalamides (e.g. N 2 -[1,1-dimethyl-2-(methylsulfonyl)ethyl]-3-iodo-N 1 -[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-1,2-benzenedicarboxamide (CAS-Reg.-No.: 272451-65-7, flubendiamide)) 21. Nereistoxin analogues (e.g. thiocyclam hydrogen oxalate, thiosultap-sodium) 22. Biologica, hormones or pheromones (e.g. azadirachtin, Bacillus spec., Beauveria spec., codlemone, Metarrhizium spec., Paecilomyces spec., thuringiensin, Verticillium spec.) 23. Compounds of unknown or non-specific mode of action 23.1 Fumigants (e.g. aluminium phosphide, methyl bromide, sulfuryl fluoride) 23.2 Selective feeding blockers (e.g. cryolite, flonicamid, pymetrozine) 23.3 Mite growth inhibitors (e.g. clofentezine, etoxazole, hexythiazox) 23.4 amidoflumet, benclothiaz, benzoximate, bifenazate, bromopropylate, buprofezin, chinomethionat, chlordimeform, chlorobenzilate, chloropicrin, clothiazoben, cycloprene, cyflumetofen, dicyclanil, fenoxacrim, fentrifanil, flubenzimine, flufenerim, flutenzin, gossyplure, hydramethylnone, japonilure, metoxadiazone, petroleum, piperonyl butoxide, potassium oleate, pyrafluprole, pyridalyl, pyriprole, sulfluramid, tetradifon, tetrasul, triarathene, verbutin further the compound 3-methyl-phenyl-propylcarbamate (Tsumacide Z), the compound 3-(5-chloro-3-pyridinyl)-8-(2,2,2-trifluoroethyl)-8-azabicyclo[3.2.1]octan-3-carbonitrile (CAS-Reg.-Nr. 185982-80-3) and the corresponding 3-endo isomer (CAS-Reg.-Nr. 185984-60-5) (cf. WO 96/37494, WO 98/25923), and preparations comprising insecticidal active plant extracts, nematodes, fungi or viruses. A mixture with other known active compounds, such as herbicides, fertilizers, growth regulators, safeners and/or semiochemicals is also possible. When used as insecticides, the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with synergistic agents. Synergistic agents are compounds, which increase the action of the active compounds, without it being necessary for the synergistic agent added to be active itself. When used as insecticides, the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms, prepared from these formulations, as a mixture with inhibitors which reduce degradation of the active compound after use in the vicinity of the plant, on the surface of parts of plants or in plant tissues. The content of the active compounds of the formula (I) of the present invention in a commercially useful application form can be varied in a wide range. The concentration of the active compounds of the formula (I) of the present invention at the time of actual usage can be, for example, in the range of 0.0000001-100% by weight, preferably 0.00001-1% by weight. The compounds of the formula (I) of the present invention can be applied by usual methods suitable to the application forms. In case of application against hygiene pests and pests of stored products, the active compounds of the present invention have a good stability against alkali on limed substrates and further show an excellent residual effectiveness on wood and soil. As already mentioned above, it is possible to treat all plants and their parts according to the invention. In a preferred embodiment, wild plant species and plant cultivars, or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and parts thereof, are treated. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated. The term “parts” or “parts of plants” or “plant parts” has been explained above. Particularly preferably, plants of the plant cultivars which are in each case commercially available or in use are treated according to the invention. Plant cultivars are to be understood as meaning plants having certain properties (“traits”) which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be cultivars, bio- or genotypes. Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, diet), the treatment according to the invention may also result in superadditive (“synergistic”) effects. Thus, for example, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity of the substances and compositions to be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, better quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products are possible which exceed the effects which were actually to be expected. The transgenic plants or plant cultivars (i.e. those obtained by genetic engineering) which are preferably to be treated according to the invention include all plants which, in the genetic modification, received genetic material which imparted particularly advantageous useful traits to these plants. Examples of such traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, better quality and/or a higher nutritional value of the harvested products, better storage stability and/or processability of the harvested products. Further and particularly emphasized examples of such traits are a better defense of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and/or viruses, and also increased tolerance of the plants to certain herbicidally active compounds. Examples of transgenic plants which may be mentioned are the important crop plants, such as cereals (wheat, rice), maize, soya beans, potatoes, cotton, tobacco, oilseed rape and also fruit plants (with the fruits apples, pears, citrus fruits and grapes), and particular emphasis is given to maize, soya beans, potatoes, cotton, tobacco and oilseed rape. Traits that are emphasized are in particular increased defense of the plants against insects, arachnids, nematodes and worms by toxins formed in the plants, in particular those formed in the plants by the genetic material from Bacillus thuringiensis (for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c, Cry2Ab, Cry3Bb and CryIF and also combinations thereof) (hereinbelow referred to as “Bt plants”). Traits that are also particularly emphasized are the increased defense of the plants against fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexius, elicitors and resistance genes and correspondingly expressed proteins and toxins. Traits that are furthermore particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulphonylureas, glyphosate or phosphinotricin (for example the “PAT” gene). The genes which impart the desired traits in question can also be present in combination with one another in the transgenic plants. Examples of “Bt plants” which may be mentioned are maize varieties, cotton varieties, soya bean varieties and potato varieties which are sold under the trade names YIELD GARD® (for example maize, cotton, soya beans), KnockOut® (for example maize), StarLink® (for example maize), Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato). Examples of herbicide-tolerant plants which may be mentioned are maize varieties, cotton varieties and soya bean varieties which are sold under the trade names Roundup Ready® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link® (tolerance to phosphinotricin, for example oilseed rape), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulphonylureas, for example maize). Herbicide-resistant plants (plants bred in a conventional manner for herbicide tolerance) which may be mentioned include the varieties sold under the name Clearfield® (for example maize). Of course, these statements also apply to plant cultivars having these genetic traits or genetic traits still to be developed, which plants will be developed and/or marketed in the future. The plants listed can be treated according to the invention in a particularly advantageous manner with the compounds of the general formula I and/or the active compound mixtures according to the invention. The preferred ranges stated above for the active compounds or mixtures also apply to the treatment of these plants. Particular emphasis is given to the treatment of plants with the compounds or mixtures specifically mentioned in the present text. Then the present invention will be described more specifically by examples. The present invention, however, should not be restricted only to them in any way. SYNTHESIS EXAMPLES Synthesis Example 1 3-(1,1-Dimethyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-1-one (0.53 g) and 1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (0.45 g) were dissolved in acetonitrile (15 ml), to which p-toluenesulfonic acid monohydrate (0.01 g) was added and the mixture was stirred at 60° C. for 3 hours. After finishing the reaction, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography to obtain N 1 -[4-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-methylphenyl]-N 2 -(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamide (0.91 g). mp. 83-87° C. Synthesis Example 2 N 1 -{4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methlylphenyl}-N 2 -(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamide (0.5 g) was dissolved in dichloromethane, to which m-chloroperbenzoic acid (0.26 g) was added and the mixture was stirred for 5 hours under ice cooling. After finishing the reaction, the mixture was washed successively with aqueous solution of sodium thiosulfate, saturated aqueous solution of sodium bicarbonate and saturated aqueous solution of sodium chloride, and dried with anhydrous magnesium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain N 1 -{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methylphenyl}-N 2 -(2-methanesulfinyl-1,1-dimethylethyl)-3-iodophthalamide (0.30 g). 1 H-NMR (CDCl 3 , ppm): 1.57 (3H, s), 1.60 (3H, s), 2.20 (3H, s), 2.30 (3H, s), 2.93 (2H, dd), 5.43 (2H, s), 6.57 (1H, s), 6.90 (1H, s), 7.0-8.2 (7H, m). Synthesis Example 3 N 1 -{4-[3,5-Bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methylphenyl}-N 2 -(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamide (0.30 g) was dissolved in dichloromethane, to which m-chloroperbenzoic acid (0.26 g) was added and the mixture was stirred at room temperature for 5 hours. After finishing the reaction, the mixture was washed successively with aqueous solution of sodium thiosulfate, saturated aqueous solution of sodium bicarbonate and saturated aqueous solution of sodium chloride, and dried with anhydrous magnesium sulfate. After distilling off the solvent, the obtained crude crystals were washed with petroleum ether to obtain N 1 -{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methylphenyl}-3-iodo-N 2 -(2-methanesulfonyl-1,1-dimethylethyl)phthalamide (0.25 g). mp. 104-107° C. Synthesis Example 4 A dioxane solution (15 ml) of 2-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methylphenyl}-4-fluoroisoindole-1,3-dione (0.94 g), (S)-1-methyl-2-methylsulfanylethylamine (0.63 g) and acetic acid (0.12 g) was refluxed for 18 hours. After cooling to room temperature, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain N 1 -{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-ylmethyl]-2-methylphenyl}-3-fluoro-N 2 -[1-(S)-1-methyl-2-methylsulfanyl-ethyl]-phthalamide (0.19 g) (compound No. 549). mp. 66-68° C. Synthesis Example 5 3-Iodo-N-(1,1-dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid (0.39 g) and N-(3-dimethylaminopropyl)-N 1 -ethylcarbonyl diimidazole hydrochloride (0.19 g) were stirred in dichloromethane (10 ml) at room temperature for 30 minutes. Then, 2-methyl-4-[1-(3-trifluoromethyl-1H-pyrazol-1-yl)-ethyl]-aniline (0.30 g) and p-toluenesulphonic acid monohydrate (0.02 g) were added thereto and the mixture was stirred at room temperature for 3 hours. After distilling off the solvent under reduced pressure, the obtained residue was purified by silica gel column chromatography to obtain N 2 -(1,1-dimethyl-2-methylsulfanyl-ethyl)-3-iodo-N 1 -{2-methyl-4-[1-(3-trifluoromethyl-1H-pyrazol-1-yl)-ethyl]-phenyl}-phthalamide (0.38 g) (compound No. 558). mp. 79-86° C. The compounds of the formula (I), according to the present invention, which can be obtained in the same manner as the above-mentioned Synthesis Examples 1 to 5 are shown in Table 1, together with the compounds obtained in the above-mentioned Synthesis Examples 1 to 5. NMR data of the compounds, whose mp. column is marked as ***, are collectively shown in Table 2, separately from Table 1. TABLE 1(I)No.R 1XYAmQR 2R 3R 4mp1C(CH 3 ) 2 CH 2 SCH 33-H2-CH 3CH 21Q1CF 3CF 3H***2C(CH 3 ) 2 CH 2 SOCH 33-H2-CH 3CH 21Q1CF 3CF 3H3C(CH 3 ) 2 CH 2 SO 2 CH 33-H2-CH 3CH 21Q1CF 3CF 3H***4CH(CH 3 )CH 2 SCH 33-H2-CH 3CH 21Q1CF 3CF 3H5CH(CH 3 )CH 2 SOCH 33-H2-CH 3CH 21Q1CF 3CF 3H6CH(CH 3 )CH 2 SO 2 CH 33-H2-CH 3CH 21Q1CF 3CF 3H7CH(CH 3 ) 23-Cl2-CH 3CH 21Q1CF 3CF 3H8C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H***9C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H80-8410C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3CF 3H183-18611CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H***12CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H76-81(S)-isomer13CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H185-19314CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3CF 3H192-194(S)-isomer15CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3CF 3H***16CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3CF 3H88-93(S)-isomer17CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q1CF 3CF 3H(S)-isomer18CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q1CF 3CF 3H(S)-isomer19CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q1CF 3CF 3H(S)-isomer20C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H21C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H22C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H23CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H24CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer25CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H26CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer27CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H28CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer29CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer30CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer31CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer32C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 2 F 533C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1HHC 2 F 534C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HHC 2 F 535CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 2 F 536CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer37CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1HHC 2 F 538CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer39CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HHC 2 F 540CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer41CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer42CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer43CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q1HHC 2 F 5(S)-isomer44CH(CH 3 ) 23-Br2-CH 3CH 21Q1CF 3CF 3H45C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3CF 3H154-16046C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3CF 3H47C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3CF 3H***48CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3CF 3H147-15549CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3CF 3H80-86(S)-isomer50CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3CF 3H51CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3CF 3H207-209(S)-isomer52CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3CF 3H***53CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3CF 3H77-85(S)-isomer54CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q1CF 3CF 3H(S)-isomer55CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q1CF 3CF 3H(S)-isomer56CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q1CF 3CF 3H(S)-isomer57C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H58C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H59C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H60CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H61CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer62CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H63CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer64CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H65CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer66CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer67CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer68CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer69C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1HHC 2 F 570C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q1HHC 2 F 571C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1HHC 2 F 572CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1HHC 2 F 573CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer74CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1HHC 2 F 575CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer76CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1HHC 2 F 577CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer78CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer79CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer80CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q1HHC 2 F 5(S)-isomer81CH(CH 3 ) 23-I2-CH 3CH 21Q1CF 3CF 3H***82C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3H83-8783C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3CF 3H***84C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3CF 3H104-10785CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3H***86CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3H85-93(S)-isomer87CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3CF 3H213-21588CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3CF 3H193-195(S)-isomer89CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3CF 3H***90CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3CF 3H87-93(S)-isomer91CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q1CF 3CF 3H79-83(S)-isomer92CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q1CF 3CF 3H(S)-isomer93CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q1CF 3CF 3H79-91(S)-isomer94C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH***95C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH96C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH***97CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH***98CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH99CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HC 3 F 7 -nH***100C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H101C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H102C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3OCHF 2H103CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H***104CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer105CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H106CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer107CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3OCHF 2H***108CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer109CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer110CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer111CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q1CF 3OCHF 2H(S)-isomer112C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1HHC 2 F 5113C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1HHC 2 F 5114C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HHC 2 F 5115CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HHC 2 F 5116CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HHC 2 F 5***(S)-isomer117CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1HHC 2 F 5118CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1HHC 2 F 5(S)-isomer119CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HHC 2 F 5120CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HHC 2 F 5(S)-isomer121CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q1HHC 2 F 5(S)-isomer122CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q1HHC 2 F 5(S)-isomer123CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q1HHC 2 F 5(S)-isomer124C(CH 3 ) 2 CH 2 SCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H125C(CH 3 ) 2 CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H126C(CH 3 ) 2 CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H127CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H128CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H177-180(S)-isomer129CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H130CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H(S)-isomer131CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H132CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q1CF 3CF 3H85-93(S)-isomer133CH(CH 3 )CH 2 SC 2 H 53-OSO2CH32-CH 3CH 21Q1CF 3CF 3H(S)-isomer134CH(CH 3 )CH 2 SOC 2 H 53-OSO2CH32-CH 3CH 21Q1CF 3CF 3H(S)-isomer135CH(CH 3 )CH 2 SO 2 C 2 H 53-OSO2CH32-CH 3CH 21Q1CF 3CF 3H(S)-isomer136CH(CH 3 ) 23-Cl2-CH 3CH 21Q2CF 3CF 3—137C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—70-72138C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—84-90139C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CF 3—88-95140CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—76-80141CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—72-81(S)-isomer142CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—186-188143CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CF 3—195-198(S)-isomer144CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CF 3—116-118145CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CF 3—95-99(S)-isomer146CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q2CF 3CF 3—73-76(S)-isomer147CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q2CF 3CF 3—180-183(S)-isomer148CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q2CF 3CF 3—66-72(S)-isomer149C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—***150C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—59-64151C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—82-87152CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—153CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—***(S)-isomer154CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—155CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—175-176(S)-isomer156CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—157CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5CF 3—82-90(S)-isomer158CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer159CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer160CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer161C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—162C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—163C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—164CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—165CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer166CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—167CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer168CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—169CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer170CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer171CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer172CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer173CH(CH 3 ) 23-Br2-CH 3CH 21Q2CF 3CF 3—174C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CF 3—77-82175C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CF 3—176C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CF 3—151-155177CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CF 3—167-169178CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CF 3—68-73(S)-isomer179CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CF 3—180CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CF 3—***(S)-isomer181CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CF 3—90-98182CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CF 3—99-112(S)-isomer183CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q2CF 3CF 3—(S)-isomer184CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q2CF 3CF 3—(S)-isomer185CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q2CF 3CF 3—(S)-isomer186C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—187C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—188C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—189CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—190CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer191CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—192CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer193CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—194CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer195CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer196CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer197CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer198C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—199C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—200C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CHF 2—201CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—202CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer203CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—204CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer205CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CHF 2—206CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer207CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer208CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer209CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer210CH(CH 3 ) 23-I2-CH 3CH 21Q2CF 3CF 3—102-105211C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CF 3—93-97212C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q2CF 3CF 3—92-93213C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CF 3—104-107214CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CF 3—92-95215CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CF 3—81-90(S)-isomer216CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2CF 3CF 3—192-195217CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2CFCF 3—192-199(S)-isomer218CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CF 3—99-104219CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CF 3—164-167(S)-isomer220CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q2CF 3CF 3—90-94(S)-isomer221CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q2CF 3CF 3—201-205(S)-isomer222CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q2CF 3CF 3—91-99(S)-isomer223C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—224C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—225C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—226CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—89-94227CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—91-104(S)-isomer228CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—229CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—190-193(S)-isomer230CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—99-116231CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5CF 3—126-132(S)-isomer232CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer233CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer234CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q2C 2 F 5CF 3—(S)-isomer235C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CHF 2—236C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q2CF 3CHF 2—237C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CHF 2—238CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CHF 2—85-88239CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2CF 3CHF 2—160-161(S)-isomer240CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2CF 3CHF 2—241CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer242CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CHF 2—***243CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2CF 3CHF 2—174-178(S)-isomer244CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer245CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer246CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q2CF 3CHF 2—(S)-isomer247C(CH 3 ) 2 CH 2 SCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—248C(CH 3 ) 2 CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—249C(CH 3 ) 2 CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—250CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—251CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—***(S)-isomer252CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—253CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—207-208(S)-isomer254CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—255CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3CH 21Q2CF 3CF 3—(S)-isomer256CH(CH 3 )CH 2 SC 2 H 53-OSO2CH32-CH 3CH 21Q2CF 3CF 3—(S)-isomer257CH(CH 3 )CH 2 SOC 2 H 53-OSO2CH32-CH 3CH 21Q2CF 3CF 3—(S)-isomer258CH(CH 3 )CH 2 SO 2 C 2 H 53-OSO2CH32-CH 3CH 21Q2CF 3CF 3—(S)-isomer259C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 3260C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 3261C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 3262CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 382-90263CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 3264CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q3OCHF 2CHF 2CF 388-99265C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 3266C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 3267C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 3268CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 3149-151269CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 3270CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q4OCHF 2CHF 2CF 381-90271C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q5CF 3CF 3OH***272C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q5CF 3CF 3OH273C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q5CF 3CF 3OH274CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q5CF 3CF 3OH275CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q5CF 3CF 3OH276CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q5CF 3CF 3OH277CH(CH 3 ) 23-I2-CH 3CH 21Q6ClClH***278C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q6HCF 3CF 3279C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q6HCF 3CF 3280C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q6HCF 3CF 3281CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q6HCF 3CF 3149-158(S)-isomer282CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q6HCF 3CF 3283CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q6HCF 3CF 3284C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—285C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—286C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—287CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—288CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—289CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q7CH 2 CF 3CF 3—290C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—291C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—292C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—293CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—294CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—295CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q8CH 2 CF 3CF 3—296C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q9CF 3CF 3—297C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q9CF 3CF 3—298C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q9CF 3CF 3—299CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9CF 3CF 3—65-79(S)-isomer300CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q9CF 3CF 3—301CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q9CF 3CF 3—302C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q10CF 3CF 3H303C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q10CF 3CF 3H304C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q10CF 3CF 3H305CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q10CF 3CF 3H306CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q10CF 3CF 3H307CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q10CF 3CF 3H308C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3O1Q10CF 3CF 3H179-181309C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3O1Q10CF 3CF 3H310C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3O1Q10CF 3CF 3H148-153311CH(CH 3 )CH 2 SCH 33-I2-CH 3O1Q10CF 3CF 3H312CH(CH 3 )CH 2 SOCH 33-I2-CH 3O1Q10CF 3CF 3H313CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3O1Q10CF 3CF 3H314C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3—0Q1CF 3CF 3H315C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3—0Q1CF 3CF 3H316C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3—0Q1CF 3CF 3H317CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1CF 3CF 3H318CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1CF 3CF 3H209-210(S)-isomer319CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1CF 3CF 3H320CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1CF 3CF 3H(S)-isomer321CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1CF 3CF 3H322CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1CF 3CF 3H218-219(S)-isomer323CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3—0Q1CF 3CF 3H(S)-isomer324CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3—0Q1CF 3CF 3H(S)-isomer325CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3—0Q1CF 3CF 3H(S)-isomer326C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3—0Q1HC 2 F 5H327C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3—0Q1HC 2 F 5H328C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HC 2 F 5H329CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1HC 2 F 5H330CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer331CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1HC 2 F 5H332CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer333CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HC 2 F 5H334CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer335CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer336CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer337CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3—0Q1HC 2 F 5H(S)-isomer338C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3—0Q1C 2 F 5HH339C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3—0Q1C 2 F 5HH340C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3—0Q1C 2 F 5HH341CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1C 2 F 5HH342CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer343CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1C 2 F 5HH344CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer345CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1C 2 F 5HH346CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer347CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer348CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer349CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3—0Q1C 2 F 5HH(S)-isomer350C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3—0Q1HHC 2 F 5351C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3—0Q1HHC 2 F 5352C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HHC 2 F 5353CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1HHC 2 F 5354CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer355CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1HHC 2 F 5356CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer357CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HHC 2 F 5358CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer359CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer360CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer361CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3—0Q1HHC 2 F 5(S)-isomer362C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3—0Q1CF 3CF 3H363C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3—0Q1CF 3CF 3H364C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3—0Q1CF 3CF 3H365CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1CF 3CF 3H366CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer367CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1CF 3CF 3H368CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer369CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1CF 3CF 3H370CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer371CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer372CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer373CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3—0Q1CF 3CF 3H(S)-isomer374C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3—0Q1HC 2 F 5H375C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3—0Q1HC 2 F 5H376C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3—0Q1HC 2 F 5H377CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1HC 2 F 5H378CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer379CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1HC 2 F 5H380CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer381CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1HC 2 F 5H382CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer383CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer384CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer385CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3—0Q1HC 2 F 5H(S)-isomer386C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3—0Q1C 2 F 5HH387C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3—0Q1C 2 F 5HH388C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3—0Q1C 2 F 5HH389CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1C 2 F 5HH390CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer391CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1C 2 F 5HH392CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer393CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1C 2 F 5HH394CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer395CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer396CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer397CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3—0Q1C 2 F 5HH(S)-isomer398C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3—0Q1HHC 2 F 5399C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3—0Q1HHC 2 F 5400C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3—0Q1HHC 2 F 5401CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1HHC 2 F 5402CH(CH 3 )CH 2 SCH 33-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer403CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1HHC 2 F 5404CH(CH 3 )CH 2 SOCH 33-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer405CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1HHC 2 F 5406CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer407CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer408CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer409CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3—0Q1HHC 2 F 5(S)-isomer410C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1CF 3CF 3H411C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1CF 3CF 3H412C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3CF 3H413CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CF 3CF 3H201414CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CF 3CF 3H192-206(S)-isomer415CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CF 3CF 3H416CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CF 3CF 3H(S)-isomer417CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3CF 3H***418CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3CF 3H(S)-isomer419CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3—0Q1CF 3CF 3H(S)-isomer420CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3—0Q1CF 3CF 3H(S)-isomer421CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3—0Q1CF 3CF 3H(S)-isomer422C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HC 2 F 5H***423C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1HC 2 F 5H424C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1HC 2 F 5H425CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1HC 2 F 5H426CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1HC 2 F 5H(S)-isomer427CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1HC 2 F 5H428CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1HC 2 F 5H(S)-isomer429CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1HC 2 F 5H430CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1HC 2 F 5H(S)-isomer431CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3—0Q1HC 2 F 5H(S)-isomer432CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3—0Q1HC 2 F 5H(S)-isomer433CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3—0Q1HC 2 F 5H(S)-isomer434C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1C 2 F 5HH***435C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1C 2 F 5HH436C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1C 2 H 5HH437CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1C 2 F 5HH438CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1C 2 F 5HH(S)-isomer439CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1C 2 F 5HH440CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1C 2 F 5HH(S)-isomer441CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1C 2 F 5HH442CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1C 2 F 5HH(S)-isomer443CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3—0Q1C 2 F 5HH(S)-isomer444CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3—0Q1C 2 F 5HH(S)-isomer445CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3—0Q1C 2 F 5HH(S)-isomer446C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HHC 2 F 5155-157447C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1HHC 2 F 5448C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1HHC 2 F 5162-168449CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1HHC 2 F 5450CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1HHC 2 F 5(S)-isomer451CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1HHC 2 F 5452CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1HHC 2 F 5(S)-isomer453CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1HHC 2 F 5454CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1HHC 2 F 5(S)-isomer455CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3—0Q1HHC 2 F 5(S)-isomer456CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3—0Q1HHC 2 F 5(S)-isomer457CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3—0Q1HHC 2 F 5(S)-isomer458C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1CH 3CF 3H459C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1CH 3CF 3H460C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1CH 3CF 3H461CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CH 3CF 3H178-180462CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CH 3CF 3H463CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CH 3CF 3H101-112464C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1CF 3CH 3H465C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1CF 3CH 3H466C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3CH 3H467CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CF 3CH 3H187-192468CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CF 3CH 3H469CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3CH 3H108-116470C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1C 2 F 5CF 3H471C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1C 2 F 5CF 3H472C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1C 2 F 5CF 3H473CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1C 2 F 5CF 3H109-111474CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1C 2 F 5CF 3H475CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1C 2 F 5CF 3H103-115476C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1CF 3HBr477C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1CF 3HBr478C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3HBr479CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CF 3HBr235-237480CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CF 3HBr481CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3HBr201-209482C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1CF 3HH483C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q1CF 3HH484C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3HH485CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q1CF 3HH173-174486CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q1CF 3HH487CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q1CF 3HH107-109488C(CH 3 ) 2 CH 2 SCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H489C(CH 3 ) 2 CH 2 SOCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H490C(CH 3 ) 2 CH 2 SO 2 CH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H491CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H492CH(CH 3 )CH 2 SCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H175-177(S)-isomer493CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H494CH(CH 3 )CH 2 SOCH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H(S)-isomer495CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H496CH(CH 3 )CH 2 SO 2 CH 33-OSO2CH32-CH 3—0Q1CF 3CF 3H(S)-isomer497C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q5C 2 F 5CF 3OH498C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q5C 2 F 5CF 3OH499C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q5C 2 F 5CF 3OH500CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q5C 2 F 5CF 3OH101-106501CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q5C 2 F 5CF 3OH502CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q5C 2 F 5CF 3OH503C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3504C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3505C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3506CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3106-116507CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3508CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q11CH 2 CF 3HCF 3127-139509C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q11CHF 2HCF 3510C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q11CHF 2HCF 3511C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q11CHF 2HCF 3512CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q11CHF 2HCF 3138-144513CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q11CHF 2HCF 3514CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q11CHF 2HCF 3515C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q12CHF 2HOCHF 2516C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3—0Q12CHF 2HOCHF 2517C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3—0Q12CHF 2HOCHF 2518CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q12CHF 2HOCHF 283-89519CH(CH 3 )CH 2 SOCH 33-I2-CH 3—0Q12CHF 2HOCHF 2520CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3—0Q12CHF 2HOCHF 292-97521CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HC 2 F 5H***522CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HC 2 F 5H***523C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1HC 2 F 5H***524C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HC 2 F 5H525CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HH526C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HH527CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HH528CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HH529C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HH***530C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HH***531CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHH532CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHH***(S)-isomer533C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHH534CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHH***535CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHH(S)-isomer536CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHH***537C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHH***538C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHH***539CH(CH 3 )CH 2 SCH(CH 3 ) 23-I2-CH 3CH 21Q1CF 3CF 3H81-83(S)-isomer540CH(CH 3 )CH 2 SOCH(CH 3 ) 23-I2-CH 3CH 21Q1CF 3CF 3H(S)-isomer541CH(CH 3 )CH 2 SO 2 CH(CH 3 ) 23-I2-CH 3CH 21Q1CF 3CF 3H(S)-isomer542CH(CH 3 )CH 2 SCH(CH 3 ) 23-Cl2-CH 3CH 21Q1CF 3CF 3H(S)-isomer543CH(CH 3 )CH 2 SCH 33-NO 22-CH 3CH 21Q1CF 3CF 3H161-171(S)-isomer544CH(CH 3 )CH 2 SOCH 33-NO 22-CH 3CH 21Q1CF 3CF 3H227-229(S)-isomer545CH(CH 3 )CH 2 SO 2 CH 33-NO 22-CH 3CH 21Q1CF 3CF 3H215-216(S)-isomer546CH(CH 3 )CH 2 SCH 33-NO 22-CH 3CH 21Q2CF 3CF 3—175-179(S)-isomer547CH(CH 3 )CH 2 SOCH 33-NO 22-CH 3CH 21Q2CF 3CF 3—225-228(S)-isomer548CH(CH 3 )CH 2 SO 2 CH 33-NO 22-CH 3CH 21Q2CF 3CF 3—206-208(S)-isomer549CH(CH 3 )CH 2 SCH 33-F2-CH 3CH 21Q1CF 3CF 3H66-68(S)-isomer550CH(CH 3 ) 23-SCH 32-CH 3CH 21Q1CF 3CF 3H***551CH(CH 3 )CH 2 SCH 33-SCH 32-CH 3CH 21Q1CF 3CF 3H(S)-isomer552CH(CH 3 )CH 2 SCH 33-SO 2 CH 32-CH 3CH 21Q1CF 3CF 3H***(S)-isomer553CH(CH 3 )CH 2 SCH 33-SCH 2 CH 32-CH 3CH 21Q1CF 3CF 3H***(S)-isomer554CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3I***(S)-isomer555CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 3HH556CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 3HH78-89(S)-isomer557CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH(CH 3 )1Q1CF 3HH150-152(S)-isomer558C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 3HH79-86559CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q1CF 3CF 3H80-91(S)-isomer560CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH(CH 3 )1Q1CF 3CF 3H(S)-isomer561CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH(CH 3 )1Q1CF 3CF 3H103-105(S)-isomer562CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H84-89(S)-isomer563CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H177-179(S)-isomer564CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H101-105(S)-isomer565C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H98-106566C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H132-136567C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH(CH 3 )1Q1CF 3CF 3H173-174568CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3CF 3—87-92(S)-isomer569CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3CF 3—***(S)-isomer570CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3CF 3—91-95(S)-isomer571CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q2CF 3CF 3—98-105(S)-isomer572CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH(CH 3 )1Q2CF 3CF 3—98-105(S)-isomer573CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH(CH 3 )1Q2CF 3CF 3—103-106(S)-isomer574CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3C 2 F 5—***(S)-isomer575CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3C 2 F 5—(S)-isomer576CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH(CH 3 )1Q2CF 3C 2 F 5—(S)-isomer577CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q2CF 3C 2 F 5—(S)-isomer578CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q2C 2 F 5CF 3—83-85(S)-isomer579CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH(CH 3 )1Q2C 2 F 5CF 3—121-124(S)-isomer580CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH(CH 3 )1Q2C 2 F 5CF 3—87-94(S)-isomer581CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q2C 2 F 5C 2 F 5—(S)-isomer582CH(CH 3 )CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q2C 2 F 5C 2 F 5—(S)-isomer583CH(CH 3 )CH 2 SCH 33-Cl2-CH 3S1Q10CF 3CF 3H(S)-isomer584CH(CH 3 )CH 2 SCH 33-I2-CH 3S1Q10CF 3CF 3H(S)-isomer585CH(CH 3 )CH 2 SCH 33-Cl2-CH 3S1Q10C 2 F 5C 2 F 5H(S)-isomer586CH(CH 3 )CH 2 SCH 33-I2-CH 3S1Q10C 2 F 5C 2 F 5H(S)-isomer587CH(CH 3 )CH 2 SCH 33-Cl2-CH 3S1Q13CF 3CF 3—(S)-isomer588CH(CH 3 )CH 2 SCH 33-I2-CH 3S1Q13CF 3CF 3—223-225(S)-isomer589CH(CH 3 )CH 2 SCH 33-I2-CH 3SO 21Q13CF 3CF 3—(S)-isomer590C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q7CH 3CHF 2—591C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q7CH 3CHF 2—592C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q7CH 3CHF 2—99-101593C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q7CH 3CHF 2—83-94594CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q14HCOCF 3H***(S)-isomer595CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q14ICOCF 3H***(S)-isomer596CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q14C 2 F 5COCF 3H***(S)-isomer597C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HHC 3 F 7 -n598C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HHC 4 F 9 -n599C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HHC 6 F 13 -n600C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q1HHC 8 F 17 -n601CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 3 F 7 -n(S)-isomer602CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 4 F 9 -n69-72(S)-isomer603CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 6 F 13 -n(S)-isomer604CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HHC 8 F 17 -n(S)-isomer605C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CH 3HC 3 F 7 -n606C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CH 3HC 4 F 9 -n607C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CH 3HC 6 F 13 -n608CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5CF 3H74-78(S)-isomer609CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5CF 3H176-177(S)-isomer610CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5CF 3H81-87(S)-isomer611CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5CF 3H(S)-isomer612CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5CF 3H(S)-isomer613CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5CF 3H(S)-isomer614CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer615CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer616CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer617CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer618CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer619CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nCF 3H(S)-isomer620C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H621C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H622C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H623C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H624C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H625C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H626CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H***(S)-isomer627CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H(S)-isomer628CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5H(S)-isomer629CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H(S)-isomer630CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H(S)-isomer631CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5C 2 F 5H(S)-isomer632CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HCl***(S)-isomer633CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HCl***(S)-isomer634CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHCl***(S)-isomer635CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HBr***(S)-isomer636CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HI***(S)-isomer637CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 2 F 573-78(S)-isomer638CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3HC 2 F 581-84(S)-isomer639CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3HC 2 F 587-90(S)-isomer640CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 2 F 5***(S)-isomer641CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3HC 2 F 5164-166(S)-isomer642CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3HC 2 F 575-85(S)-isomer643CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 3 F 7 -n73-75(S)-isomer644CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 3 F 7 -n86-88(S)-isomer645CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 4 F 9 -n79-82(S)-isomer646CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 3HC 4 F 9 -n73-76(S)-isomer647CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 3HC 4 F 9 -n83-88(S)-isomer648CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 4 F 9 -n88-92(S)-isomer649CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 3HC 4 F 9 -n84-90(S)-isomer650CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 3HC 4 F 9 -n75-78(S)-isomer651CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5***(S)-isomer652CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5124-125(S)-isomer653CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 588-91(S)-isomer654CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5***(S)-isomer655CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 587-92(S)-isomer656CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5100-107(S)-isomer657CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n64-65(S)-isomer658CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n***(S)-isomer659CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n78-81(S)-isomer660CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n***(S)-isomer661CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n83-85(S)-isomer662CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n92-96(S)-isomer663CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n72-74(S)-isomer664CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n84-88(S)-isomer665CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 578-85(S)-isomer666CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 578-85(S)-isomer667CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n70-74(S)-isomer668CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n73-77(S)-isomer669CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n77-82(S)-isomer670CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n86-90(S)-isomer671CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n81-84(S)-isomer672CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n147-148(S)-isomer673CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HC 2 F 5CF 3(S)-isomer674CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HC 2 F 5CF 3(S)-isomer675CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HC 2 F 5C 2 F 5***(S)-isomer676CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HC 2 F 5C 2 F 5(S)-isomer677C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—678C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—679C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—680CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—681CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—***(S)-isomer682CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—683CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—162-164(S)-isomer684CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—685CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—103-106(S)-isomer686CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer687CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer688CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer689C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—690C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—691C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—692CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—693CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer694CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—695CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer696CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—697CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3HC 21Q2C 2 F 5C 2 F 5—(S)-isomer698CH(CH 3 )CH 2 SC 2 H 53-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer699CH(CH 3 )CH 2 SOC 2 H 53-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer700CH(CH 3 )CH 2 SO 2 C 2 H 53-Br2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer701C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—702C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—703C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—704CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—705CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer706CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—707CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer708CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—709CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer710CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer711CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer712CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q2C 2 F 5C 2 F 5—(S)-isomer713C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2C 3 F 7 -nCF 3—714CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 3 F 7 -nCF 3—***(S)-isomer715CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 3 F 7 -nCF 3—(S)-isomer716CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 3 F 7 -nC 2 F 5—(S)-isomer717CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q2C 3 F 7 -nC 2 F 5—(S)-isomer718C(CH 3 ) 2 CH 2 SCH 33-F2-CH 3CH 21Q1CF 3CF 3H719C(CH 3 ) 2 CH 2 SOCH 33-F2-CH 3CH 21Q1CF 3CF 3H720C(CH 3 ) 2 CH 2 SO 2 CH 33-F2-CH 3CH 21Q1CF 3CF 3H721CH(CH 3 )CH 2 SOCH 33-F2-CH 3CH 21Q1CF 3CF 3H(S)-isomer722CH(CH 3 )CH 2 SO 2 CH 33-F2-CH 3CH 21Q1CF 3CF 3H(S)-isomer723CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1HHC 4 F 9 -n63-69(S)-isomer724CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HHC 4 F 9 -n95-97(S)-isomer725CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1HCF 3C 3 F 7 -n76-81(S)-isomer726CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1HCF 3C 3 F 7 -n***(S)-isomer727CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HCF 3C 3 F 7 -n***(S)-isomer728CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1HC 2 F 5C 2 F 568-72(S)-isomer729CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1HC 2 F 5C 2 F 5***(S)-isomer730CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CHF 2CHF 2H***(S)-isomer731C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HCF 3732CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HCF 3(S)-isomer733C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HCF 2 CHF 2734CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HCF 2 CHF 2(S)-isomer735C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 4 F 9 -n736CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 4 F 9 -n737CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 6 F 13 -n78-82(S)-isomer738CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3HC 8 F 17 -n79-82(S)-isomer739CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 3CF 3CF 3(S)-isomer740C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5741CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5***(S)-isomer742CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 564-67(S)-isomer743CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 583-89(S)-isomer744C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HCF 3745CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HCF 375-80(S)-isomer746CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer747CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer748CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer749C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5750C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5751C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5752CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5753CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5754CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5755CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q1C 2 F 5HC 2 F 595-100(S)-isomer756CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q1C 2 F 5HC 2 F 5(S)-isomer757CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3—0Q1C 2 F 5HC 2 F 589-94(S)-isomer758CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH(CH 3 )1Q1C 2 F 5HC 2 F 5(S)-isomer759CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3—0Q1C 2 F 5HC 2 F 5195-195(S)-isomer760CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH(CH 3 )1Q1C 2 F 5HC 2 F 5(S)-isomer761CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 570-74(S)-isomer762CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 579-84(S)-isomer763CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q1C 2 F 5HC 2 F 5185-188(S)-isomer764C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q1C 2 F 5HC 3 F 7 -n765C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n766C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n767C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n768CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n769C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n770CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n771CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n81-85(S)-isomer772CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n(S)-isomer773C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5FCF 3774CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5FCF 3775CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5FCF 3142-146(S)-isomer776CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 2 F 5FCF 3(S)-isomer777CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 2 F 5FCF 3(S)-isomer778CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5CH 3C 2 F 5***(S)-isomer779CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 2 F 5C 2 F 5C 2 F 5(S)-isomer780C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5781C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5782C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5783CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5784CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 581-83(S)-isomer785CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 585-90(S)-isomer786C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH(CH 3 )1Q1C 3 F 7 -nHC 3 F 7 -n787C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n788C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n789C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n790CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n791CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n792CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n793CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nC 3 F 7 -nH74-78(S)-isomer794CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nC 3 F 7 -nH72-76(S)-isomer795CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q1C 3 F 7 -nC 3 F 7 -nH149-150(S)-isomer796CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CHFCF 3CF 3—66-69(S)-isomer797CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CHFCF 3CF 3—80-85(S)-isomer798CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CHFCF 3CF 3—81-86(S)-isomer799CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2CF 2 CHF 2CF 2 CHF 2—***(S)-isomer800CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q2CF 2 CHF 2CF 2 CHF 2—159-163(S)-isomer801CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q2CF 2 CHF 2CF 2 CHF 2—77-83(S)-isomer802C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q2C 3 F 7 -nC 3 F 7 -n—803CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2C 4 F 9 -nH—218-210(S)-isomer804CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q2SC 3 F 7 -nCF 3—73-76(S)-isomer805CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer806CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer807CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer808C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q9CF 3CF 3—809C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q9CF 3CF 3—810C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9CF 3CF 3—811CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9CF 3CF 3—812CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q9CF 3CF 3—813CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9CF 3CF 3—814CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q9CF 3CF 3—(S)-isomer815CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9CF 3CF 3—(S)-isomer816CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q9CF 3CF 3—(S)-isomer817CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q9CF 3CF 3—(S)-isomer818CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q9CF 3CF 3—(S)-isomer819C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—820C(CH 3 ) 2 CH 2 SOCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—821C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—822CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—823CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—824CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—825CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer826CH(CH 3 )CH 2 SOCH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer827CH(CH 3 )CH 2 SO 2 CH 33-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer828CH(CH 3 )CH 2 SC 2 H 53-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer829CH(CH 3 )CH 2 SOC 2 H 53-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer830CH(CH 3 )CH 2 SO 2 C 2 H 53-Cl2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer831C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5C 2 F 5—832CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5C 2 F 5—833CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9C 2 F 5C 2 F 5—(S)-isomer834C(CH 3 ) 2 CH 2 SCH 33-Cl2-CH 3CH 21Q9C 3 F 7 -nCF 3—835CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q9C 3 F 7 -nCF 3—(S)-isomer836CH(CH 3 )CH 2 SCH 33-Cl2-CH 3S1Q18CF 3CH 3—(S)-isomer837CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q19CF 3CH 3—(S)-isomer838CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q17CF 3H—839CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q15HC 2 F 5—840CH(CH 3 )CH 2 SCH 33-Cl2-CH 3CH 21Q15HC 2 F 5—71-75(S)-isomer841CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q20CF 3——(S)-isomer842CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q16C 2 F 5——843CH(CH 3 )CH 2 SCH 33-Cl2-CH 3—0Q16C 3 F 7 -n——844C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3HC 2 F 5845C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3HC 4 F 9 -n846CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1CF 3HC 4 F 9 -n847C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5848C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5849C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5850C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5851CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5852CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5853CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1C 2 F 5HC 2 F 5854C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n855CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n856CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5857C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n858C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n859C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n860CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n861CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n862CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n863C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q9CF 3CF 3—864C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q9CF 3CF 3—865C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q9CF 3CF 3—866CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q9CF 3CF 3—867CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q9CF 3CF 3—868CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q9CF 3CF 3—869C(CH 3 ) 2 CH 2 SCH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—870C(CH 3 ) 2 CH 2 SOCH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—871C(CH 3 ) 2 CH 2 SO 2 CH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—872CH(CH 3 )CH 2 SCH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—873CH(CH 3 )CH 2 SOCH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—874CH(CH 3 )CH 2 SO 2 CH 33-Br2-CH 3CH 21Q9C 2 F 5CF 3—875CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1HHC 4 F 9 -n80-85(S)-isomer876CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1HHC 4 F 9 -n160-162(S)-isomer877CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1HHC 4 F 9 -n85-89(S)-isomer878CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CHF 2CHF 2H***(S)-isomer879C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HCF 3880C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HCF 2 CHF 2881CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HCF 2 CHF 2(S)-isomer882C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 2 F 5883CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 2 F 5884C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 4 F 9 -n885CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3HC 4 F 9 -n886C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3CF 3887CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 3CF 3CF 3888C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1CF 2 CHF 2HC 2 F 5889C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5890CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5(S)-isomer891CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5(S)-isomer892CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1CF 2 CHF 2HC 2 F 5(S)-isomer893C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HCF 3894CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer895CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer896CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HCF 2 CHF 2(S)-isomer897C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q1C 2 F 5HC 2 F 5898C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5899C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5900C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5901CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5902CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5903CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5904CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5(S)-isomer905CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5(S)-isomer906CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q1C 2 F 5HC 2 F 5(S)-isomer907C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n908C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n909C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n910CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 3 F 7 -n911C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n912CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n913CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n90-96(S)-isomer914CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 2 F 5HC 4 F 9 -n92-97(S)-isomer915C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 2 F 5FCF 3916C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5917CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5918CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5919CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 5920CH(CH 3 )CH 2 SOCH 33-I2-CHCH 21Q1C 3 F 7 -nHC 2 F 589-96(S)-isomer921CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 2 F 592-96(S)-isomer922C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n923C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n924C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n925CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n926CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n927CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q1C 3 F 7 -nHC 3 F 7 -n928C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q2C 3 F 7 -nC 3 F 7 -n—929CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer930CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer931CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q6CF 3CF 3CF 3(S)-isomer932C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q9CF 3CF 3—933CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9CF 3CF 3—934CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q9CF 3CF 3—935CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q9CF 3CF 3—936CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q9CF 3CF 3—(S)-isomer937CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q9CF 3CF 3—(S)-isomer938CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q9CF 3CF 3—(S)-isomer939CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q9CF 3CF 3—(S)-isomer940CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q9CF 3CF 3—(S)-isomer941C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q9C 2 F 5CF 3—942C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—943C(CH 3 ) 2 CH 2 SOCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—944C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—945CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—946CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—947CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—948CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer949CH(CH 3 )CH 2 SOCH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer950CH(CH 3 )CH 2 SO 2 CH 33-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer951CH(CH 3 )CH 2 SC 2 H 53-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer952CH(CH 3 )CH 2 SOC 2 H 53-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer953CH(CH 3 )CH 2 SO 2 C 2 H 53-I2-CH 3CH 21Q9C 2 F 5CF 3—(S)-isomer954C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH(CH 3 )1Q9C 2 F 5C 2 F 5—955C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5C 2 F 5—956CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5C 2 F 5—957CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9C 2 F 5C 2 F 5—(S)-isomer958C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q9C 3 F 7 -nCF 3—959CH(CH 3 )CH 2 SCH 33-I2-CH 3CH 21Q9C 3 F 7 -nCF 3—(S)-isomer960C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3S1Q18CF 3CH 3—961C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q19CF 3CH 3—962C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q17CF 3H—963C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3CH 21Q15HC 2 F 5—964C(CH 3 ) 2 CH 2 SCH 33-I2-CH 3—0Q20CF 3——965CH(CH 3 )CH 2 SCH 33-I2-CH 3—0Q16CF 3——966C(CH 3 ) 2 CH 2 SCH 33-Cl2-FCH 21Q1CF 3CF 3H967C(CH 3 ) 2 CH 2 SOCH 33-Cl2-FCH 21Q1CF 3CF 3H968C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-FCH 21Q1CF 3CF 3H969C(CH 3 ) 2 CH 2 SCH 33-Cl2-ClCH 21Q1CF 3CF 3H970C(CH 3 ) 2 CH 2 SOCH 33-Cl2-ClCH 21Q1CF 3CF 3H971C(CH 3 ) 2 CH 2 SO 2 CH 33-Cl2-ClCH 21Q1CF 3CF 3H972CH(CH 3 ) 2 SCH 33-Cl2-ClCH 21Q1CF 3CF 3H973CH(CH 3 )CH 2 SOCH 33-Cl2-ClCH 21Q1CF 3CF 3H974CH(CH 3 )CH 2 SO 2 CH 33-Cl2-ClCH 21Q1CF 3CF 3H975CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q1CF 3CF 3H(S)-isomer976CH(CH 3 )CH 2 SOCH 33-Cl2-ClCH 21Q1CF 3CF 3H(S)-isomer977CH(CH 3 )CH 2 SO 2 CH 33-Cl2-ClCH 21Q1CF 3CF 3H(S)-isomer978CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q1C 2 F 5CF 3H(S)-isomer979CH(CH 3 )CH 2 SOCH 33-Cl2-ClCH 21Q1C 2 F 5CF 3H(S)-isomer980CH(CH 3 )CH 2 SO 2 CH 33-Cl2-ClCH 21Q1C 2 F 5CF 3H(S)-isomer981C(CH 3 ) 2 CH 2 SCH 33-Cl2-ClCH 21Q1CF 3HC 2 F 5982C(CH 3 ) 2 CH 2 SCH 33-Cl2-ClCH 21Q1CF 3HC 3 F 7 -n983C(CH 3 ) 2 CH 2 SCH 33-Cl2-ClCH 21Q1CF 3HC 4 F 9 -n984C(CH 3 ) 2 CH 2 SCH 33-Cl2-ClCH 21Q1CF 3HC 6 F 13 -n985CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q1C 2 F 5HC 2 F 5(S)-isomer986CH(CH 3 )CH 2 SOCH 33-Cl2-ClCH 21Q1C 2 F 5HC 2 F 5(S)-isomer987CH(CH 3 )CH 2 SO 2 CH 33-Cl2-ClCH 21Q1C 2 F 5HC 2 F 5(S)-isomer988CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q1C 2 F 5HC 3 F 7 -n(S)-isomer989CH(CH 3 )CH 2 SOCH 33-Cl2-ClCH 21Q1C 2 F 5HC 3 F 7 -n(S)-isomer990CH(CH 3 )CH 2 SO 2 CH 33-Cl2-ClCH 21Q1C 2 F 5HC 3 F 7 -n(S)-isomer991CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q2CF 3CF 3—(S)-isomer992CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q2C 2 F 5CF 3—(S)-isomer993CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q9CF 3CF 3—(S)-isomer994CH(CH 3 )CH 2 SCH 33-Cl2-ClCH 21Q9C 2 F 5CF 3—(S)-isomer995C(CH 3 ) 2 CH 2 SCH 33-I2-FCH 21Q1CF 3CF 3H***996C(CH 3 ) 2 CH 2 SOCH 33-I2-FCH 21Q1CF 3CF 3H997C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-FCH 21Q1CF 3CF 3H113-115998C(CH 3 ) 2 CH 2 SCH 33-I2-ClCH 21Q1CF 3CF 3H157-159999C(CH 3 ) 2 CH 2 SOCH 33-I2-ClCH 21Q1CF 3CF 3H1000C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-ClCH 21Q1CF 3CF 3H129-1341001C(CH 3 ) 2 CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5CF 3H1002C(CH 3 ) 2 CH 2 SOCH 33-I2-ClCH 21Q1C 2 F 5CF 3H1003C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-ClCH 21Q1C 2 F 5CF 3H1004C(CH 3 ) 2 CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5C 2 F 5H1005C(CH 3 ) 2 CH 2 SOCH 33-I2-ClCH 21Q1C 2 F 5C 2 F 5H1006C(CH 3 ) 2 CH 2 SO 2 CH 33-I2-ClCH 21Q1C 2 F 5C 2 F 5H1007CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5HC 2 F 5(S)-isomer1008CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5HC 3 F 7 -n(S)-isomer1009CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5HC 4 F 9 -n(S)-isomer1010CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q1C 2 F 5HC 6 F 13 -n(S)-isomer1011CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q2CF 3CF 3—(S)-isomer1012CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q2C 2 F 5CF 3—(S)-isomer1013CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q2C 2 F 5C 2 F 5—(S)-isomer1014CH(CH 3 )CH 2 SCH 33-I2-ClCH 21Q2C 3 F 7 -nCF 3—(S)-isomer TABLE 2No.11H-NMR(CDCl3, ppm): 1.4 (6H, s), 2.0 (3H, s), 2.3 (3H, s), 2.9 (2H, s), 5.4 (2H, s), 6.2 (1H, s), 6.9 (1H,s), 7.3-8.7 (8H, m)31H-NMR(CDCl3, ppm): 1.5 (6H, s), 2.2 (3H, s), 2.6 (3H, s), 3.7 (2H, s), 5.4 (2H, s), 6.4 (1H, s), 6.9 (1H,s), 7.3-8.2 (8H, m)81H-NMR(CDCl3, ppm): 1.4 (6H, s), 2.0 (3H, s), 2.3 (3H, s), 2.9 (2H, s), 5.4 (2H, s), 6.1 (1H, s), 6.9 (1H,s), 7.3-8.4 (7H, m)111H-NMR(CDCl3, ppm): 1.2 (3H, d), 1.9 (3H, s), 2.3 (3H, s), 2.7 (2H, dd), 4.2 (1H, m), 5.4 (2H, s), 6.4(1H, d), 6.9 (1H, s), 7.3-8.4 (7H, m)151H-NMR(CDCl3, ppm): 1.3 (3H, d), 2.2 (3H, s), 2.8 (3H, s), 3.2 (2H, m), 4.6 (1H, m), 5.4 (2H, s), 6.4(1H, d), 6.9-8.4 (8H, m)471H-NMR(CDCl3, ppm): 1.6 (6H, s), 2.3 (3H, s), 2.5 (3H, s), 3.5 (2H, s), 5.4 (2H, s), 6.6 (1H, s), 6.9 (1H,s), 7.3-8.2 (7H, m)521H-NMR(CDCl3, ppm): 1.4 (3H, d), 2.2 (3H, s), 2.7 (3H, s), 3.2 (2H, m), 4.4 (1H, m), 5.4 (2H, s),6.9-8.2 (9H, m)811H-NMR(CDCl3, ppm): 1.1 (6H, d), 2.2 (3H, s), 4.2 (1H, m), 5.3 (2H, s), 5.9 (1H, d), 6.9-8.2 (8H, m)831H-NMR(CDCl3, ppm): 1.57 (3H, s), 1.60 (3H, s), 2.20 (3H, s), 2.30 (3H, s), 2.93 (2H, dd), 5.43 (2H, s),6.57 (1H, s), 6.90 (1H, s), 7.0-8.2 (7H, m)851H-NMR(CDCl3, ppm): 1.2 (3H, d), 1.8 (3H, s), 2.2 (3H, s), 2.6 (2H, dd), 4.2 (1H, m), 5.3 (2H, s), 6.5(1H, d), 6.9 (1H, s), 7.3-8.4 (7H, m)891H-NMR(CDCl3, ppm): 1.4 (3H, d), 2.2 (3H, s), 2.7 (3H, s), 3.2 (2H, m), 4.5 (1H, m), 5.3 (2H, s), 6.6(1H, d), 6.9-7.9 (8H, m)941H-NMR(CDCl3, ppm): 1.57 (3H, s), 1.60 (3H, s), 2.20 (3H, s), 2.30 (3H, s), 2.93 (2H, dd), 5.43 (2H, s),6.57 (1H, s), 6.90 (1H, s), 7.0-8.2 (7H, m)961H-NMR(CDCl3, ppm): 1.63 (6H, s), 2.27 (3H, s), 2.50 (3H, s), 3.47 (2H, s), 5.30 (2H, s), 6.23 (1H, s),6.57 (1H, s), 7.0-8.1 (8H, m)971H-NMR(CDCl3, ppm): 1.27 (3H, d), 1.93 (3H, s), 2.30 (3H, s), 2.63 (2H, m), 4.33 (1H, m), 5.37 (2H,s), 6.07 (1H, m), 6.60 (1H, s), 6.9-8.2 (8H, m)991H-NMR(CDCl3, ppm): 1.50 (3H, d), 2.27 (3H, s), 2.70 (3H, s), 3.0-3.5 (2H, m), 4.60 (1H, m), 5.37 (2H,s), 6.5-8.0 (10H, m)1031H-NMR(CDCl3, ppm): 1.27 (3H, d), 1.93 (3H, s), 2.30 (3H, s), 2.60 (2H, m), 4.33 (1H, m), 5.20 (2H,s), 6.17 (1H, s), 6.47 (1H, t), 7.1-8.3 (8H, m)1071H-NMR(CDCl3, ppm): 1.50 (3H, d), 1.93 (3H, s), 2.30 (3H, s), 2.60 (2H, m), 4.33 (1H, m), 5.20 (2H,s), 6.17 (1H, s), 6.47 (1H, t), 6.67 (1H, m), 7.0-8.1 (7H, m)1161H-NMR(CDCl3, ppm): 1.2 (3H, d), 1.9 (3H, s), 2.2 (3H, s), 2.6 (2H, dd), 4.2 (1H, m), 5.2 (2H, s), 6.4(1H, d), 7.0-8.3 (9H, m)1491H-NMR(CDCl3, ppm): 1.34 (6H, s), 1.95 (3H, s), 2.33 (3H, s), 2.86 (2H, s), 5.48 (2H, s), 6.11 (1H, s),7.56-7.00 (4H, m), 7.84-7.72 (1H, m), 8.23 (1H, d), 8.49 (1H, s)1531H-NMR(CDCl3, ppm): 1.22 (3H, d), 2.05 (3H, s), 2.30 (3H, s), 2.61-2.53 (2H, m), 4.40-4.29 (1H, m),5.44 (2H, s), 6.19 (1H, d), 7.17 (2H, t), 7.54-7.48 (2H, m), 7.73 (1H, d), 8.15 (1H, d), 8.44 (1H, s)1801H-NMR(CDCl3, ppm): 1.3 (3H, d), 2.2 (3H, s), 2.3 (3H, s), 2.8 (2H, d), 4.5 (1H, m), 5.4 (2H, s), 7.1-8.3(8H, m)2421H-NMR(CDCl3, ppm): 1.4 (3H, d), 2.2 (3H, s), 2.8 (3H, s), 3.2 (2H, m), 4.6 (1H, m), 5.5 (2H, s),6.2-8.2 (9H, m)2511H-NMR(CDCl3, ppm): 1.25 (3H, d), 1.95 (3H, s), 2.28 (3H, s), 2.63-2.51 (2H, m), 3.28 (3H, s),4.36-4.26 (1H, m), 5.43 (2H, s), 6.38 (1H, d, J = 9.3 Hz), 7.39-7.16 (2H, m), 7.62-7.53 (2H,m), 7.81-7.74 (1H, m), 8.38 (1H, s)2711H-NMR(CDCl3, ppm): 1.47 (6H, s), 2.00 (3H, s), 2.30 (3H, s), 2.83 (2H, s), 3.30 (1H, m), 4.2-4.6 (4H,m), 6.07 (1H, s), 7.1-8.2 (7H, m)2771H-NMR(CDCl3, ppm): 1.1 (6H, d), 2.2 (3H, s), 4.1 (1H, m), 5.0 (2H, s), 6.0 (1H, d), 7.0-8.4 (8H, m)4171H-NMR(CDCl3, ppm): 1.5 (3H, d), 2.3 (3H, s), 2.8 (3H, s), 3.2 (2H, dd), 4.7 (1H, m), 6.5 (1H, m), 7.0(1H, s), 7.3-8.3 (6H, m)4221H-NMR(CDCl3, ppm): 1.47 (6H, s), 2.03 (3H, s), 2.40 (3H, s), 2.87 (2H, s), 6.03 (1H, s), 6.80 (1H, m),7.1-8.6 (8H, m)4341H-NMR(CDCl3, ppm): 1.40 (6H, s), 2.03 (3H, s), 2.40 (3H, s), 2.87 (2H, s), 6.07 (1H, s), 6.77 (1H, m),7.2-8.5 (8H, m)5211H-NMR(CDCl3, ppm): 1.23 (3H, d), 1.90 (3H, s), 2.26 (3H, s), 2.50-2.67 (2H, m), 4.10-4.50 (1H, m),5.37 (2H, s), 6.15 (1H, d), 6.60 (1H, bs), 6.90-7.20 (3H, m), 7.57 (1H, bs), 7.70 (1H, d),7.80-8.23 (3H, m)5221H-NMR(CDCl3, ppm): 1.50 (3H, d), 2.30 (3H, s), 2.70 (3H, s), 2.97-3.50 (2H, m), 4.56 (1H, m), 5.43(2H, s), 6.60-8.03(10H, m)5231H-NMR(CDCl3, ppm): 1.40 (6H, s), 1.98 (3H, s), 2.30 (3H, s), 2.73 (2H, s), 5.40 (2H, s), 6.03 (1H, bs),6.60-7.20 (4H, m), 7.50-8.20 (5H, m)5291H-NMR(CDCl3, ppm): 1.42 (6H, s), 1.98 (3H, s), 2.30 (3H, s), 2.71 (2H, s), 5.30 (2H, s), 6.03 (1H, bs),6.52 (1H, d), 7.03-7.35 (4H, m),7.73 (1H, d), 7.93 (1H, d), 8.10-8.40 (2H, m)5301H-NMR(CDCl3, ppm): 1.63 (6H, s), 2.30 (3H, s), 2.57 (3H, s), 3.47 (2H, s), 5.30 (2H, s), 6.40 (1H, bs),6.57 (1H, d), 7.03-8.1 7 (8H, m)5321H-NMR(CDCl3, ppm): 1.30 (4H, dd), 1.97 (3H, s), 2.28 (3H, s), 2.73-2.42 (2H, m), 4.37-4.28 (1H, m),5.28 (2H, s), 6.42 (1H, d), 6.55 (1H, d), 7.09 (2H, t), 7.42-7.39 (2H, m), 7.51 (1H, d), 7.70 (1H,t), 8.02 (1H, d), 8.49 (1H, d)5341H-NMR(CDCl3, ppm): 1.24 (3H, d), 1.93 (3H, s), 2.30 (3H, s), 2.50-2.66 (2H, m), 4.23-4.40 (1H, m),5.32 (2H, s), 6.16 (1H, d), 6.54 (1H, d), 7.06 (1H, bs), 7.11 (1H, d), 7.22 (1H, t), 7.40 (1H, d),7.78 (1H, d), 7.97 (1H, d), 8.17 (1H, d), 8.30 (1H, bs)5361H-NMR(CDCl3, ppm): 1.50 (3H, d), 2.28 (3H, s), 2.73 (3H, s), 2.97-3.50 (2H, m), 4.60 (1H, m), 5.30(2H, s), 6.53 (1H, d), 6.73 (1H, d), 7.00-8.07(8H, m)5371H-NMR(CDCl3, ppm): 1.40(6H, s), 1.98 (3H, s), 2.31 (3H, s), 2.81 (2H, s), 5.32 (2H, s), 6.08 (1H, bs),6.54 (1H, d), 7.04 (1H, bs) 7.11 (1H, d), 7.20 (1H, t), 7.38 (1H, d), 7.79 (1H, d), 7.96 (1H, d),8.22 (1H, d), 8.38 (1H, bs)5381H-NMR(CDCl3, ppm): 1.66(6H, s), 2.30 (3H, s), 2.60 (3H, s), 3.52 (2H, s), 5.30 (2H, s), 6.47 (1H, bs),6.57 (1H, d), 7.03-8.23 (8H, m)5501H-NMR(CDCl3, ppm): 1.48 (6H, d), 2.21 (3H, s), 2.48 (3H, s), 4.13 (1H, m), 5.42 (2H, s), 6.18(1H, d),6.91 (1H, s), 7.1-7,6 (6H, m), 8.08 (1H, d)5521H-NMR(CDCl3, ppm): 1.17 (3H, d), 1.89 (3H, s), 2.29 (3H, s), 2.42 (1H, dd), 2.60 (1H, dd), 3.29 (3H,s), 4.24 (1H, m), 5.42 (2H, s), 6.41 (1H, d),6.92 (1H, s), 7.1-7.2 (2H, m), 7.6-8.2 (5H, m)5531H-NMR(CDCl3, ppm): 1.21 (3H, d), 1.32 (3H, t), 1.95 (3H, s), 2.29 (3H, s), 2.51 (1H, dd), 2.60 (1H,dd), 3.00 (2H, q), 4.31 (1H, m), 5.41 (2H, s),6.28 (1H, d), 6.91 (1H, s), 7.1-7.2 (2H, m), 7.4-7.6 (3H, m), 8.09 (1H, d), 8.34 (1H, s)5541H-NMR(CDCl3, ppm): 1.25 (5H, dd), 1.91 (3H, s), 2.29 (3H, s), 2.60-2.54 (2H, m), 4.32-4.27 (1H, m),5.44 (2H, s), 6.40 (1H, d), 7.06 (2H, d, J = 7.5 Hz), 7.19-7.12 (1H, m), 7.71 (1H, d), 7.94-7.91(1H, m), 8.08 (1H, d), 8.36 (1H, s)5691H-NMR(CDCl3, ppm): 8.50 (1H, m), 7.95 (1H, m), 7.79-7.49 (4H, m), 7.44-7.38 (1H, m), 7.22 (1H, m),5.75 (1H, q), 4.38 (1H, m), 2.79 (2H, m), 2.29 (3H, s), 2.20 (3H, s), 2.00 (3H, d), 1.43-1.18 (3H,d)5741H-NMR(CDCl3, ppm): 1.31 (3H, d), 1.95 (3H, s), 2.30 (3H, s), 2.61-2.57 (2H, m), 4.37-4.27 (1H, m),5.79-5.73 (1H, m), 6.48 (1H, d), 7.02 (1H, s), 7.25-7.21 (2H, m), 7.52-7.36 (3H, m), 7.84-7.69(2H, m), 8.04 (1H, d), 8.50 (1H, s)5941H-NMR(CDCl3, ppm): 1.22 (3H, d), 1.93 (3H, s), 2.26 (3H, s), 2.61-2.55 (2H, m), 4.36-4.27 (1H, m),5.49 (2H, d), 6.07 (1H, d), 6.34-6.30 (1H, m), 6.98 (2H, d), 7.13 (1H, t), 7.27-7.22 (3H, m),7.79 (1H, d), 7.97 (1H, dd), 8.08 (1H, d), 8.23 (1H, s)5951H-NMR(CDCl3, ppm): 1.25 (3H, d), 1.94 (3H, s), 2.27 (3H, s), 2.60-2.54 (2H, m), 4.34-4.25 (1H, m),5.49 (2H, d), 6.42 (1H, d), 7.04-6.99 (2H, m), 7.21-7.14 (2H, m), 7.35-7.32 (1H, m), 7.72 (1H,d), 7.93 (1H, dd), 8.05 (1H, d), 8.36 (1H, s)5961H-NMR(CDCl3, ppm): 1.24 (3H, d), 1.97 (3H, s), 2.33 (3H, s), 2.63-2.54 (2H, m), 4.35-4.30 (1H, m),5.52 (2H, s), 6.05 (1H, d), 7.02-7.00 (2H, m), 7.26-7.21 (1H, m), 7.35-7.32 (1H, m), 7.42-7.39(1H, m), 7.80 (1H, t), 7.98 (1H, d), 8.18 (1H, t), 8.32 (1H, d)6261H-NMR(CDCl3, ppm): 1.22 (3H, d), 1.92 (3H, s), 2.30 (3H, s), 2.54 (1H, dd), 2.61 (1H, dd), 4.32 (1H,m), 5.46 (2H, s), 6.23 (1H, m), 6.94 (1H, s), 7.0-7.1 (2H, m), 7.45 (1H, m), 7.54 (1H, d), 7.72(1H, d), 8.07 (1H, d), 8.38 (1H, bs)6321H-NMR(CDCl3, ppm): 1.26 (3H, dd), 1.96 (3H, s), 2.32 (3H, s), 2.61-2.55 (2H, m), 4.34-4.29 (1H, m),5.22 (2H, s), 6.22 (1H, d), 7.21-7.13 (3H, m), 7.36 (1H, d), 7.78 (1H, d), 7.97 (1H, dd), 8.16(1H, d), 8.35 (1H, s)6331H-NMR(CDCl3, ppm): 1.23 (3H, dd), 1.97 (3H, s), 2.31 (3H, s), 2.61-2.56 (2H, m), 4.37-4.32 (1H, m),5.25 (2H, s), 6.13 (1H, d), 7.11 (2H, dd), 7.37 (1H, t), 7.48 (1H, dd), 7.61-7.53 (1H, m), 7.79(1H, dt), 8.15 (1H, d), 8.43 (1H, d)6341H-NMR(CDCl3, ppm): 1.25 (4H, dd), 1.98 (3H, s), 2.33 (3H, s), 2.61-2.56 (2H, m), 8.41 (1H, s),4.38-4.31 (1H, m), 5.24 (2H, s), 6.17 (1H, d), 7.13-7.11 (2H, m), 7.38 (1H, s), 7.46 (1H, t), 7.56(1H, dd), 7.79 (1H, t), 8.14 (1H, d)6351H-NMR(CDCl3, ppm): 1.26 (3H, dd), 1.94 (3H, s), 2.31 (3H, s), 2.61-2.52 (2H, m), 4.33-4.29 (1H, m),5.24 (2H, s), 6.34 (1H, d), 7.21-7.11 (3H, m), 7.39 (1H, d), 7.75 (1H, d), 7.95 (1H, dd), 8.13(1H, d, )8.38 (1H, s)6361H-NMR(CDCl3, ppm): 1.25 (3H, dd), 1.93 (2H, s), 2.31 (3H, s), 2.65-2.52 (2H, m), 4.32-4.29 (1H, m),5.26 (2H, s), 6.40 (1H, d), 7.21-7.11 (3H, m), 8.39 (1H, s), 7.42 (1H, s), 7.74 (1H, d), 7.94 (1H,d), 8.11 (1H, d)6401H-NMR(CDCl3, ppm): 1.29 (3H, dd), 1.95 (3H, s), 2.32 (3H, s), 2.62-2.54 (2H, m), 4.34-4.27 (1H, m),5.31 (2H, s), 6.21 (1H, d), 7.96 (1H, d), 8.19 (1H, t), 7.21-7.13 (3H, m), 7.62 (1H, s), 7.78 (1H,d), 8.37 (1H, d)6511H-NMR(CDCl3, ppm): 1.24 (3H, dd), 1.96 (3H, s), 2.31 (3H, s), 2.60-2.55 (2H, m), 4.36-4.31 (1H, m),5.31 (2H, s), 6.34 (1H, d), 7.16-7.14 (2H, m), 7.43 (1H, t), 7.53 (1H, dd), 7.64 (1H, s), 7.71(1H, d), 8.12 (1H, d), 8.50 (1H, s)6541H-NMR(CDCl3, ppm): 1.26 (3H, dd), 1.93 (3H, s), 2.34 (3H, d), 2.62-2.55 (2H, m), 4.34-4.29 (1H, m),5.31 (2H, s), 6.23 (1H, d), 7.24-7.14 (3H, m), 7.63 (1H, s), 7.78 (1H, d), 7.97 (1H, dd), 8.20(1H, d), 8.37 (1H, s)6581H-NMR(CDCl3, ppm): 1.44-1.38 (3H, m), 2.35-2.30 (6H, m), 2.90-2.77 (2H, m), 4.56-4.48 (1H, m),5.32 (2H, s), 7.18-7.14 (3H, m), 7.44-7.37 (1H, m), 7.56-7.52 (1H, m), 7.67-7.64 (2H, m),8.10-8.07 (1H, m), 8.44-8.39 (1H, m)6601H-NMR(CDCl3, ppm): 1.25 (4H, dd), 1.90 (3H, s), 2.31 (3H, s), 2.63-2.55 (2H, m), 4.37-4.28 (1H, m),5.34 (2H, s), 6.12 (1H, d), 7.22-7.15 (2H, m), 7.63 (1H, d), 7.83 (1H, t), 7.98 (1H, dt), 8.25(1H, t), 8.34 (1H, s)6751H-NMR(CDCl3, ppm): 1.23 (3H, d), 1.97 (3H, s), 2.33 (3H, s), 2.63-2.54 (2H, m), 4.38-4.29 (1H, m),5.41 (2H, s), 6.21 (1H, d), 7.09 (2H, d), 7.44 (1H, t), 7.54 (1H, d), 7.73 (1H, d), 7.84 (1H, s),8.07 (1H, d), 8.38 (1H, s)6811H-NMR(CDCl3, ppm): 1.25 (3H, d), 1.95 (3H, s), 2.32 (3H, s), 2.62-2.54 (2H, m), 4.36-4.32 (1H, m),5.52 (2H, s), 6.13 (1H, d), 7.18-7.16 (2H, m), 7.57-7.47 (2H, m), 7.76 (1H, d), 8.17 (1H, d),8.41 (1H, s)7141H-NMR(CDCl3, ppm): 1.24 (3H, d), 1.99 (3H, s), 2.30 (3H, s), 2.64-2.52 (2H, m), 4.38-4.29 (1H, m),5.49 (2H, s), 6.15 (1H, d), 7.17-7.15 (2H, m), 7.57-7.43 (2H, m), 7.75 (1H, d), 8.17 (1H, d),8.41 (1H, s)7261H-NMR(CDCl3, ppm): 1.45-1.37 (3H, m), 2.32-2.30 (6H, m), 2.87-2.83 (2H, m), 4.61-4.46 (1H, m),5.44 (2H, s), 6.90-6.88 (1H, m), 7.12-7.09 (2H, m), 7.45-7.42 (1H, m), 7.55-7.52 (1H, m),7.68-7.66 (1H, m), 7.79-7.77 (1H, m), 8.06-8.04 (1H, m), 8.32-8.24 (1H, m)7271H-NMR(CDCl3, ppm): 1.44 (3H, d), 2.30 (3H, s), 2.75 (3H, s), 3.24-3.21 (2H, m), 4.62-4.53 (1H, m),5.44 (2H, s), 6.87-6.85 (1H, m), 7.08-7.06 (2H, m), 7.42-7.32 (1H, m), 7.50-7.47 (1H, m),7.60-7.57 (1H, m), 7.77 (1H, s), 7.91-7.87 (1H, m), 8.17-8.14 (1H, m)7291H-NMR(CDCl3, ppm): 1.45 (3H, d), 2.29 (3H, s), 2.75 (3H, s), 3.34-3.12 (2H, m), 4.59-4.54 (1H, m),5.38 (2H, s), 6.86 (1H, d), 7.09-7.06 (2H, m), 7.43-7.33 (1H, m), 7.52-7.46 (1H, m), 7.59 (1H,d), 7.84 (1H, s), 7.90 (1H, d), 8.15 (1H, s)7301H-NMR(CDCl3, ppm): 1.23 (3H, d), 1.96 (3H, s), 2.29 (3H, s), 2.5-2.7 (2H, m), 4.31 (1H, m), 5.34(2H, s), 6.31 (1H, d), 6.4-7.2 (5H, s), 7.4-7.8 (3H, m), 8.06 (1H, d), 8.41 (1H, bs)7411H-NMR(CDCl3, ppm): 1.26 (3H, d), 1.95 (3H, s), 2.18 (3H, s), 2.30 (3H, s), 2.66-2.48 (2H, m),4.39-4.20 (1H, m), 5.31 (2H, s), 6.25 (1H, d), 7.07-7.01 (2H, m), 7.44-7.41 (2H, m), 7.55-7.51(2H, m), 7.71 (1H, d), 8.01 (1H, d), 8.32 (1H, s)7781H-NMR(CDCl3, ppm): 1.31 (3H, d), 1.95 (3H, s), 2.33 (3H, t), 2.61-2.56 (2H, m), 4.40-4.29 (1H, m),5.28 (2H, s), 6.50-6.11 (2H, m), 7.15-7.12 (2H, m), 7.45-7.42 (1H, m), 7.55-7.52 (1H, m), 7.64(1H, s), 7.72 (1H, d), 8.12 (1H, d), 8.50 (1H, s)7991H-NMR(CDCl3, ppm): 1.23 (3H, d), 1.93 (3H, s), 2.32 (3H, s), 2.56 (2H, m), 4.22 (1H, m), 5.52 (2H,s), 6.55-6.02 (3H, m), 7.21 (2H, m), 7.57-7.43 (2H, m), 7.76 (1H, d), 8.15 (1H, d), 8.39 (1H, s)1H-NMR(CDCl3, ppm): 1.24 (3H, d), 1.94 (3H, s), 2.28 (3H, s), 2.52 (1H, dd), 2.62 (1H, dd), 4.30 (1H,m), 5.38 (2H, s), 6.4-7.2 (7H, m), 7.72 (1H, d), 7.93 (1H, d), 8.06 (1H, d), 8.41 (1H, bs)1H-NMR(CDCl3, ppm): 1.40 (6H, s), 1.93 (3H, s), 2.77 (2H, s), 5.40 (2H, s), 5.93 (1H, bs), 6.87-7.23(4H, m), 7.63-7.95 (2H, m), 8.35-8.65 (2H, m) Synthesis Example 6 Starting Material 3-Methyl-4-nitrobenzyl chloride (1.81 g), 3,5-bis(trifluoromethyl)-1H-pyrazole (2.0 g) and potassium carbonate (1.63 g) were stirred in DMF (20 ml) at 60° C. for 1 hour. After finishing the reaction, water (100 ml) was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride (100 ml) and dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-3,5-bis-(trifluoromethyl)-1H-pyrazole (3.3 g). 1 H-NMR (CDCl 3 , ppm): 2.59 (3H, s), 5.50 (2H, s), 6.90 (1H, s), 7.1-7.2 (2H, m), 8.00 (1H, d). Synthesis Example 7 Starting Material To a mixture of 1-(3-methyl-4-nitrobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (1.4 g), ammonium acetate (30.5 g), acetone (60 ml) and water (30 ml), 20% aqueous solution of titanium trichloride (27.5 g) was added at room temperature and the mixture was stirred at room temperature for 12 hours. After finishing the reaction, the mixture was extracted with ethyl acetate, washed with saturated aqueous solution of sodium chloride and dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (1.19 g). 1 H-NMR (CDCl 3 , ppm): 2.14 (3H, s), 3.66 (2H, m), 5.32 (2H, s), 6.62 (1H, d), 6.89 (1H, s), 6.8-7.1 (2H, m). Synthesis Example 8 Starting Material 1-(3-Methyl-4-nitrobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (17.66 g) and iron powder (13.69 g) were heated and stirred in acetic acid (150 ml) at 40° C. for 5 hours. After finishing the reaction, an insoluble matter was filtered with Celite and the filtrate was concentrated under the reduced pressure. To the residue, 1N aqueous solution of sodium hydrate (200 ml) and ethyl acetate (200 ml) were added. The organic layer was separated, washed with water, and then, dried with anhydrous magnesium sulfate. After distilling off the solvent, 1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (13.0 g), which was the same as that obtained in Synthesis Example 7, was obtained. Synthesis Example 9 Starting Material 3-Fluorophthalic anhydride (4.98 g) and 1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (9.70 g) were refluxed in acetic acid (43 ml) for 3 hours. After finishing the reaction, the acetic acid was distilled off under the reduced pressure and the obtained crude crystals were washed with t-butyl methyl ether to obtain the aimed 2-{4-[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl-methyl]-2-methylphenyl}-4-fluoroisoindol-1,3-dione (10.80 g). mp. 158-159° C. Synthesis Example 10 Starting Material 3-Methyl-4-nitrobenzyl chloride (0.56 g), 5-(difluoromethyl)-1,2-dihydro-2-methyl-3H-1,2,4-(triazol)-3-one (0.45 g) and potassium carbonate (0.61 g) were stirred in DMF (10 ml) at 50° C. for 5 hours. After finishing the reaction, the reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride and then dried with anhydrous magnesium sulfate, and the solvent was distilled off under the reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain the aimed 5-difluoromethyl-2-methyl-4-(3-methyl-4-nitrobenzyl)-2,4-dihydro-[1,2,4]triazol-3-one (0.45 g). 1 H-NMR (CDCl 3 , ppm): 2.5 (3H, s), 3.5 (3H, s), 4.9 (2H, s), 6.4 (1H, t), 7.2-7.3 (2H, m), 7.8-7.9 (1H, m). Synthesis Example 11 Starting Material 3-Methyl-4-nitrobenzyl chloride (0.43 g), 3-heptafluoropropylsulfanyl-5-trifluoromethyl-1H-(1,2,4)-triazole (0.70 g), tetrabutylammonium iodide (0.09 g), 18-crown-6 (0.06 g) and potassium carbonate (0.48 g) were refluxed in acetonitrile (10 ml) for 2 hours. After cooling, the reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 3-heptafluoropropylsulfanyl-1-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-1H-(1,2,4)-triazole (0.30 g). 1 H-NMR (CDCl 3 , ppm): 2.64 (3H, s), 5.62 (2H, s), 7.31-7.25 (2H, m), 8.05-7.86 (1H, m) Synthesis Example 12 Starting Material To a mixture of 3-heptafluoropropylsulfanyl-1-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-1H-(1,2,4)-triazole (0.3 g), ammonium acetate (4.8 g), acetone (20 ml) and water (10 ml), 20% aqueous solution of titanium trichloride (4.3 g) was added at room temperature and the mixture was stirred at room temperature for 12 hours. After finishing the reaction, the mixture was extracted with ethyl acetate, washed with saturated aqueous solution of sodium chloride and dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 4-(3-heptafluoropropylsulfanyl-5-trifluoromethyl-[1,2,4]triazol-1-ylmethyl)-2-methyl-phenylamine (0.28 g) 1 H-NMR (CDCl 3 , ppm): 2.17 (3H, s), 4.16 (1H, brs), 5.40 (2H, s), 6.63-6.59 (2H, m), 7.13-6.99 (1H, m). Synthesis Example 13 Starting Material An acetonitrile solution (30 ml) of 3-trifluoromethyl-1H-pyrazole (5.0 g), dicerium ammonium nitrate (10.0 g) and iodine (5.6 g) was refluxed for 1 hour. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 4-iodo-3-trifluoromethyl-1H-pyrazole (9.3 g). 1 H-NMR (CDCl 3 , ppm): 7.77 (1H, s). Synthesis Example 14 Starting Material 3-Methyl-4-nitrobenzyl chloride (0.77 g), 4-iodo-3-trifluoromethyl-1H-pyrazole (0.99 g) and potassium carbonate (0.63 g) were stirred in DMF (10 ml) at 60° C. for 1 hour. After cooling, the reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 4-iodo-1-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-1H-pyrazole (1.0 g). 1 H-NMR (CDCl 3 , ppm): 2.62 (3H, s), 5.36 (2H, s), 7.21-7.18 (2H, m), 7.52 (1H, s), 7.98 (1H, d). Synthesis Example 15 Starting Material 4-Iodo-1-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-1H-pyrazole (2.06 g), copper powder (0.95 g), iodopentafluoroethane (4.92 g) and DMF (13 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 130-135° C. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (50 ml) and an insoluble matter was filtered with Celite and washed with ethyl acetate. The filtrate was concentrated under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-4-pentafluoroethyl-3-trifluoromethyl-1H-pyrazole (1.39 g) 1 H-NMR (CDCl 3 , ppm): 2.63 (3H, s), 5.38 (2H, s), 7.21-7.27 (2H, m), 7.74 (1H, s), 8.00 (1H, d). Synthesis Example 16 Starting Material 3-Methyl-4-nitrobenzyl chloride (8.57 g), 4-iodo-3-pentafluoroethyl-1H-pyrazole (16.00 g) and potassium carbonate (7.66 g) were stirred in DMF (70 ml) at 70° C. for 1 hour. After cooling, the reaction solution was poured into water and extracted with ethyl acetate. The organic phase was washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with sodium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 4-iodo-1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole (4.60 g). 1 H-NMR (CDCl 3 , ppm): 2.60 (3H, s), 5.38 (2H, s), 7.22-7.15 (2H, m), 7.53 (1H, s), 7.98 (1H, d). Synthesis Example 17 Starting Material 4-Iodo-1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole (1.84 g), (trifluoromethyl)trimethylsilane (1.14 g), copper(I) iodide (1.52 g), potassium fluoride (0.28 g) were stirred in DMF (8 ml) at 100° C. for 8 hours. After cooling, the mixture was poured into water and extracted with ethyl acetate. The combined organic phase was washed with saturated aqueous solution of sodium chloride. After drying the organic layer with sodium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitro-benzyl)-3-pentafluoroethyl-4-trifluoromethyl-1H-pyrazole (0.32 g). 1 H-NMR (CDCl 3 , ppm): 2.61 (3H, s), 5.41 (2H, s), 7.31-7.18 (2H, m), 7.78 (1H, s), 8.00 (1H, d). Synthesis Example 18 Starting Material 4-Iodo-1-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-1H-pyrazole (2.06 g), copper powder (0.95 g), heptafluoro-1-iodopropane (2.96 g) and DMF (14 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 130-135° C. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (50 ml) and an insoluble matter was filtered with Celite and washed with ethyl acetate. The filtrate was concentrated under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-4-pentafluoropropyl-3-trifluoromethyl-1H-pyrazole (0.80 g). 1 H-NMR (CDCl 3 , ppm): 2.62 (3H, s), 5.42 (2H, s), 7.19-7.20 (2H, m), 7.74 (1H, s), 8.02 (1H, d). Synthesis Example 19 Starting Material 4-Iodo-1-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-1H-pyrazole (2.47 g), copper powder (1.14 g), nonafluoro-1-iodobutane (4.15 g) and DMF (16 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 130-135° C. After cooling to room temperature, the reaction mixture was diluted with toluene (50 ml) and an insoluble matter was filtered with Celite and washed with toluene. The filtrate was concentrated under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-4-nonafluorobutyl-3-trifluoromethyl-1H-pyrazole (1.50 g). 1 H-NMR (CDCl 3 , ppm): 2.62 (3H, s), 5.42 (2H, s), 7.18-7.24 (2H, m), 7.74 (1H, s), 8.00 (1H, d). Synthesis Example 20 Starting Material An acetonitrile solution (20 ml) of 3-trifluoromethyl-1H-pyrazole (1.0 g), dicerium ammonium nitrate (2.0 g) and bromine (0.7 g) was refluxed for 2 hours. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 4-bromo-3-trifluoromethyl-1H-pyrazole (1.6 g). 1 H-NMR (CDCl 3 , ppm): 7.73 (1H, s), 12.86 (1H, brs). Synthesis Example 21 Starting Material 3-Methyl-4-nitrobenzyl chloride (0.77 g), 4-bromo-3-trifluoromethyl-1H-pyrazole (0.90 g) and potassium carbonate (0.57 g) were stirred in DMF (10 ml) at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-4-bromo-3-trifluoromethyl-1H-pyrazole (0.9 g). 1 H-NMR (CDCl 3 , ppm): 2.58 (3H, s), 5.35 (2H, s), 7.24-7.21 (2H, m), 7.49 (1H, s), 7.98 (1H, d). Synthesis Example 22 Starting Material An acetonitrile solution (20 ml) of 3-trifluoromethyl-1H-pyrazole (0.5 g), dicerium ammonium nitrate (1.0 g) and N-chlorosuccinimide (0.7 g) was refluxed for 3 hours. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying an organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 4-chloro-3-trifluoromethyl-1H-pyrazole (0.9 g). 1 H-NMR (CDCl 3 , ppm): 7.80 (1H, s). Synthesis Example 23 Stating Material 3-Methyl-4-nitrobenzyl chloride (0.82 g), 4-chloro-3-trifluoromethyl-1H-pyrazole (0.63 g) and potassium carbonate (0.61 g) were stirred in DMF (10 ml) at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-4-chloro-3-trifluoromethyl-1H-pyrazole (0.98 g). 1 H-NMR (CDCl 3 , ppm): 2.62 (3H, s), 5.33 (2H, s), 7.21-7.19 (2H, m), 7.46 (1H, s), 7.98 (1H, d). Synthesis Example 24 Starting Material 2-(Trifluoroacetyl)-1H-pyrrole (0.97 g) was added to DMF solution (10 ml) of 60% sodium hydride (0.16 g) and the mixture was stirred at room temperature for 30 minutes. 3-Methyl-4-nitrobenzyl chloride (1.0 g) was added thereto and the mixture was stirred at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrobenzyl)-2-(trifluoroacetyl)-1H-pyrrole (1.53 g). 1 H-NMR (CDCl 3 , ppm): 2.55 (3H, s), 5.59 (2H, s), 6.44-6.41 (1H, m), 6.99 (1H, d), 7.04 (1H, s), 7.22-7.19 (1H, m), 7.35-7.32 (1H, m), 7.93 (1H, d). Synthesis Example 25 Starting Material An acetonitrile solution (20 ml) of 2-(trifluoroacetyl)-1H-pyrrole (0.5 g), dicerium ammonium nitrate (0.84 g) and iodine (0.47 g) was refluxed for 2 hours. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 4-iodo-2-(trifluoroacetyl)-1H-pyrrole (0.6 g). 1 H-NMR (CDCl 3 , ppm): 7.28-7.35 (2H, m), 9.52 (1H, brs). Synthesis Example 26 Starting Material 3-Methyl-4-nitrobenzyl chloride (0.63 g), 4-iodo-2-(trifluoroacetyl)pyrrole (0.89 g) and potassium carbonate (0.57 g) were stirred in DMF (10 ml) at room temperature for 2 hours. The reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 4-iodo-1-(3-methyl-4-nitrobenzyl)-2-trifluoroacetyl-1H-pyrrole (0.45 g). 1 H-NMR (CDCl 3 , ppm): 2.60 (3H, s), 5.56 (2H, s), 7.05-7.12 (2H, m), 7.21 (1H, d), 7.39 (1H, s), 7.94 (1H, d). Synthesis Example 27 Starting Material 4-Iodo-1-(3-methyl-4-nitrobenzyl)-2-trifluoroacetyl-1H-pyrrole (1.75 g), copper powder (5.08 g), iodopentafluoroethane (5.92 g) and DMSO (6 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 120° C. After finishing the reaction, the reaction mixture was poured into ice water and an insoluble matter was filtered with Celite, and then, it was extracted with ethyl acetate. The extracted solution was washed with water and then dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrophenyl)-4-pentafluoroethyl-1H-pyrrole (1.35 g). 1 H-NMR (CDCl 3 , ppm): 2.59 (3H, s), 5.62 (2H, s), 7.00-7.10 (2H, m), 7.43-7.50 (2H, m), 7.96 (1H, d). Some specific examples of other processes to synthesize the compounds of the aforementioned formula (IX) are shown below. Synthesis Example 28 Starting Material To a toluene suspension of ethyl 4,4,4-trifluoroacetoacetone (5.0 g), sodium hydride (1.1 g) was slowly added and the mixture was stirred for 1 hour. After adding 4-chloromethyl-2-methyl-1-nitro-benzene (5.5 g) and potassium iodide dissolved in acetone (0.5 g), the reaction solution was refluxed for 5 hours. After cooling, the solvent was distilled off under reduced pressure. The residue was suspended in ethyl acetate and washed with 1N aqueous solution of hydrochloric acid. After drying the organic layer with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain ethyl 4,4,4-trifluoro-2-(3-methyl-4-nitro-benzyl)-3-oxo-butyrate (6.3 g). n D 20 1.4970 Synthesis Example 29 Starting Material Ethyl 4,4,4-trifluoro-2-(3-methyl-4-nitro-benzyl)-3-oxo-butyrate (2.0 g), hydrazine monohydrate (0.5 g) and a small amount of p-toluenesulfonic acid were dissolved in toluene, and the mixture was refluxed for 4 hours. After cooling, the solvent was distilled off under reduced pressure. The residue was suspended in ethyl acetate and washed with 1N aqueous solution of hydrochloric acid. After drying the organic layer with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 4-(3-methyl-4-nitro-benzyl)-5-trifluoromethyl-2,4-dihydro-pyrazol-3-one (1.0 g). 1 H-NMR (DMSO-d 6 , 90 MHz): δ 2.2 (3H, s), 3.8 (2H, s), 7.0 (1H, d, J=5.5 Hz), 7.2 (1H, s), 7.8 (1H, d, J=5.5 Hz), 11.2 (1H, brs). Synthesis Example 30 Starting Material To a DMF suspension of 4-(3-methyl-4-nitro-benzyl)-5-trifluoromethyl-2,4-dihydro-pyrazol-3-one (1.0 g) and potassium carbonate (1.5 g), chlorodifluoromethane (5.7 g) was sealed in by using a balloon. After 5 hours, after the gas in the solution was saturated, the vessel was tightly closed and the mixture was stirred at 50° C. for 5 hours. After cooling, the solvent was distilled off and the obtained residue was dissolved in ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 5-difluoromethoxy-1-difluoromethyl-4-(3-methyl-4-nitro-benzyl)-3-trifluoromethyl-1H-pyrazole (IX-1) (0.5 g) and 3-difluoromethoxy-j-difluoromethyl-4-(3-ethyl-4-nitro-benzyl)-5-trifluoromethyl-1H-pyrazole (IX-2) (0.4 g) respectively. (IX-1): n D 20 1.4780, (IX-2): n D 20 1.4855. Synthesis Example 31 Starting Material (3-Methyl-4-nitrophenyl)-hydrazine (3.0 g) and hexafluoroacetylacetone (3.7 g) were dissolved in toluene and the solution was refluxed for 6 hours. After cooling, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrophenyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (5.6 g). n D 20 1.4890. Synthesis Example 32 Starting Material (3-Methyl-4-nitro-phenyl)-hydrazine (2.0 g) and 1,1,1,5,5,6,6,6-octafluoro-2,4-hexanedione (3.1 g) were dissolved in toluene and the solution was refluxed for 6 hours. After cooling, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitro-phenyl)-3-pentafluoroethyl-5-trifluoromethyl-1H-pyrazole (IX-3) (3.0 g) and 2-(3-methyl-4-nitro-phenyl)-5-pentafluoroethyl-3-trifluoromethyl-3,4-dihydro-2H-pyrazol-3-ol (IX-4) (0.5 g), respectively. (IX-3): n D 20 1.4690, (IX-4): 1 H-NMR (CDCl 3 , 90 MHz): δ 2.6 (3H, s), 3.3 (1H, br d, J=16 Hz), 3.7 (1H, br d, J=16 Hz), 4.1 (1H, s), 7.2 (2H, m), 7.8 (1H, d, J=7.8 Hz). Synthesis Example 33 Starting Material To a THF suspension of 1-(3-methyl-4-nitro-phenyl)-ethanone (2.0 g), sodium hydride (0.6 g) was slowly added and the mixture was stirred for 1 hour. After adding ethyl trifluoroacetate (1.6 g), the reaction mixture was refluxed for 5 hours. After cooling, the solvent was distilled off under reduced pressure. The residue was suspended in ethyl acetate and washed with 1N aqueous solution of hydrochloric acid. After drying the organic layer with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 4,4,4-trifluoro-1-(3-methyl-4-nitro-phenyl)-butane-1,3-dione (2.5 g). 1 H-NMR (CDCl 3 , 90 MHz): δ 2.6 (3H, s), 6.5 (1H, s), 7.7-8.1 (3H, m). Synthesis Example 34 Starting Material A toluene solution of 4,4,4-trifluoro-1-(3-methyl-4-nitro-phenyl)-butane-1,3-dione (1.8 g), 2,2,2-trifluoroethylhydrazine (1.2 g) and a catalytic amount of p-toluenesulfonic acid were refluxed for 6 hours. After cooling, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 3-(3-methyl-4-nitro-phenyl)-1-(2,2,2-trifluoro-ethyl)-5-trifluoro-methyl-1H-pyrazole (IX-5) (1.1 g) and 5-(3-methyl-4-nitro-phenyl)-1-(2,2,2-trifluoro-ethyl)-3-trifluoromethyl-1H-pyrazole (1-6) (0.5 g), respectively. (IX-5) mp; 98-104° C., (IX-6) mp; 50-53° C. Synthesis Example 35 Starting Material To a dichloromethane solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (10 g) and dimethylaminopyridine (17 g), a dichloromethane solution of 3-methyl-4-nitro-benzoyl chloride (14 g) was added dropwise under ice cooling. After stirring at room temperature for 3 hours and then adding 100 ml of ethanol, the mixture was refluxed for 2 hours. After cooling, the solvent was distilled off under the reduced pressure. The residue was dissolved in ethyl acetate and washed with 1N aqueous solution of hydrochloric acid. After drying the organic layer with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain ethyl 3-(3-methyl-4-nitro-phenyl)-3-oxo-propionate (12.4 g). mp; 207-211° C. Synthesis Example 36 Starting Material To an ethanol solution of ethyl 3-(3-methyl-4-nitro-phenyl)-3-oxo-propionate (3.0 g), hydrazine monohydrate (0.9 g) and a small amount of p-toluenesulfonic acid were added and the mixture was refluxed for 5 hours. After cooling, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 5-(3-methyl-4-nitro-phenyl)-2,4-dihydro-pyrazol-3-one (2.6 g). mp; 218-219° C. Synthesis Example 37 Starting Material To a DMF suspension of 5-(3-methyl-4-nitro-phenyl)-2,4-dihydro-1H-pyrazol-3-one (2.0 g) and potassium carbonate (6.3 g), chlorodifluoromethane (8.7 g) was sealed in by using a balloon. After 5 hours, after the gas in the solution was saturated, the vessel was tightly closed and the mixture was stirred at 50° C. for 5 hours. After cooling, the solvent was distilled off and the obtained residue was dissolved in ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying with sodium sulfate, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography to obtain 5-difluoromethoxy-1-difluoromethyl-3-(3-methyl-4-nitro-phenyl)-1H-pyrazole (IX-7) (0.7 g) and 3-difluoromethoxy-1-difluoromethyl-5-(3-methyl-4-nitro-phenyl)-1H-pyrazole (IX-8) (0.5 g), respectively. (IX-7) mp; 80-82° C., (IX-8) mp; 99-100° C. Synthesis Example 38 Starting Material To an ethanol solution (60 ml) of hydrazine monohydrate (5.00 g), an ethanol solution (20 ml) of 3-methyl-4-nitrobenzyl chloride (3.71 g) was added dropwise while refluxing it, and the mixture was continuously refluxed for 6 hours. After finishing the reaction, the solvent was distilled off and (3-methyl-4-nitrobenzyl)-hydrazine (3.50 g) was obtained. 1 H-NMR (CDCl 3 , ppm): 2.60 (3H, s), 2.65-3.35 (3H, m), 3.95 (2H, s), 7.20-7.40 (2H, m), 7.98 (1H, d). Synthesis Example 39 Starting Material (3-Methyl-4-nitrobenzyl)-hydrazine (1.81 g) and 5-ethoxy-1,1,1,2,2-pentafluoro-4-penten-3-one (2.18 g) were refluxed in ethanol (60 ml) for 8 hours, and p-toluenesulfonic acid (0.10 g) was added thereto and the mixture was further refluxed for 6 hours. After finishing the reaction, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography (mixed solvent of n-hexane and ethyl acetate) to obtain 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole (0.96 g) as the first elution portion and 1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole (0.50 g) as the second elution portion. (IX-9): 1 H-NMR (CDCl 3 , ppm): 2.61 (3H, s), 5.49 (2H, s), 6.70 (1H, bs), 7.05-7.15 (2H, m), 7.66 (1H, bs), 7.94 (1H, d). (IX-10): 1 H-NMR (CDCl 3 , ppm): 2.64 (3H, s), 5.40 (2H, s), 6.63 (1H, d), 7.07-7.20 (2H, m), 7.52 (1H, d), 7.95 (1H, d). Synthesis Example 40 Starting Material A mixture of 5-fluoro-2-nitrotoluene (2.33 g), 4-iodo-1H-pyrazole (2.91 g) and potassium carbonate (2.49 g) was heated and stirred in DMF (30 ml) at 140° C. for 4 hours. After cooling to room temperature, the reaction mixture was poured into ice water to separate out crystals. The obtained crystals were filtered, washed with water and dried, and 4-iodo-1-(3-methyl-4-nitrophenyl)-1H-pyrazole (4.60 g) was obtained. 1 H-NMR (CDCl 3 , ppm): 2.70 (3H, s), 7.50-7.70 (3H, m), 7.95-8.15 (2H, m). Synthesis Example 41 Starting Material 4-Iodo-1-(3-methyl-4-nitrophenyl)-1H-pyrazole (1.98 g), copper powder (1.14 g), iodopentafluoroethane (8.85 g) and DMSO (9 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 100° C. After finishing the reaction, the reaction mixture was poured into ice water and an insoluble matter was filtered with Celite, and then, it was extracted with ethyl acetate. The extracted solution was washed with water and dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 1-(3-methyl-4-nitrophenyl)-4-pentafluoroethyl-1H-pyrazole (0.72 g). 1 H-NMR (CDCl 3 , ppm): 2.70 (3H, s), 7.60-7.73 (2H, m), 7.93 (1H, s), 8.13 (1H, d), 8.23 (1H, s). Synthesis Example 42 Starting Material To a suspension of methanol (300 ml) of 3-methyl-4-nitroacetophenone (26.88 g), sodium borohydride (8.51 g) was added at 0° C. over a period of 1 hour. The mixture was further stirred at room temperature for 8 hours. After finishing the reaction, the reaction mixture was poured into ice water (1,000 ml) and extracted with ether. The organic layer was washed with saturated aqueous solution of sodium chloride and dried with anhydrous magnesium sulfate. After distilling off the solvent, the aimed 1-(3-methyl-4-nitrophenyl)-ethanol (23.33 g) was obtained. 1 H-NMR (CDCl 3 , ppm): 1.51 (3H, d), 1.98 (1H, d), 2.62 (3H, s), 4.90-5.01 (1H, m), 7.28-7.35 (2H, m), 7.98 (1H, d). Synthesis Example 43 Starting Material Into a THF solution (35 ml) of 1-(3-methyl-4-nitrophenyl)-ethanol (5.44 g) and triethylamine (3.95 g), a THF solution (10 ml) of methanesulfonyl chloride (3.48 g) was added dropwise at 5° C. over a period of 30 minutes. Further, the mixture was stirred at room temperature for 8 hours. After finishing the reaction, the solvent was distilled off and the residue was dissolved in ethyl acetate (100 ml). It was washed with 2N aqueous solution of hydrochloric acid and saturated aqueous solution of sodium bicarbonate and then dried with anhydrous magnesium sulfate. After distilling off the solvent, the aimed 1-(3-methyl-4-nitrophenyl)-ethyl methanesulfonate (5.80 g) was obtained. 1 H-NMR (CDCl 3 , ppm): 1.74 (3H, d), 2.65 (3H, s), 2.95 (3H, s), 5.76 (1H, q), 7.35-7.45 (2H, m), 8.01 (1H, d). Synthesis Example 44 Starting Material 1-(3-Methyl-4-nitrophenyl)-ethyl methanesulfonate (2.59 g), 3-trifluoromethyl-1H-pyrazole (1.09 g), potassium carbonate (1.66 g) and 18-crown-6 (0.26 g) were refluxed in acetonitrile (100 ml) for 6 hours. After finishing the reaction, water (100 ml) was added to the mixture and extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium bicarbonate and then dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography to obtain 1-[1-(3-methyl-4-nitrophenyl)-ethyl]-3-trifluoromethyl-1H-pyrazole (1.60 g). 1 H-NMR (CDCl 3 , ppm): 1.95 (3H, d), 2.59 (3H, s), 5.59 (1H, q), 6.57 (1H, bs), 7.13-7.20 (2H, m), 7.47 (1H, bs), 8.00 (1H, d). Synthesis Example 45 Starting Material Ethyl pentafluoropropylenate (14.6 g) and hydrazine monohydrate (3.6 g) were refluxed in tetrahydrofuran (300 ml) for 1 hour. After cooling to room temperature, trifluoroacetamidine (10.0 g) was added dropwise to the mixture and it was refluxed for 3 hours. After finishing the reaction, saturated aqueous solution of sodium hydrogen carbonate was added thereto and the mixture was extracted with ethyl acetate. After drying the organic layer with anhydrous magnesium sulfate, the solvent was distilled off to obtain crude 3-pentafluoroethyl-5-trifluoromethyl-1H-(1,2,4)-triazole (7.9 g). Synthesis Example 46 Starting Material 1-(3-Methyl-4-nitrophenyl)-ethyl methanesulfonate (2.5 g), 3-pentafluoroethyl-5-trifluoromethyl-1H-(1,2,4)-triazole (2.2 g), potassium carbonate (1.6 g) and 18-crown-6 (0.26 g) were refluxed in acetonitrile (100 ml) for 6 hours. After finishing the reaction, water (100 ml) was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride (100 ml) and then dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography (mixed solvent of n-hexane and ethyl acetate) to obtain (IX-11) 1-([1-(3-methyl-4-nitro-phenyl)-ethyl]-5-pentafluoroethyl-3-trifluoromethyl-1H-(1,2,4)-triazole (0.95 g) as the first elution portion and (IX-12) 1-([1-(3-methyl-4-nitro-phenyl)-ethyl]-3-pentafluoroethyl-5-trifluoromethyl-1H-(1,2,4)-triazole (1.35 g) as the second elution portion. (IX-11) 1 H-NMR (CDCl 3 ) δ: 8.03-7.97 (1H, m), 7.37 (2H, t, J=5.4 Hz), 5.86 (1H, q, J=7.0 Hz), 2.62 (3H, s), 2.00 (311, d, J=7.0 Hz). (X-12) 1 H-NMR (CDCl 3 ) δ: 7.98 (1H, d; J=8.2 Hz), 7.34 (2H, t, J=7.1 Hz), 5.81 (1H, q, J=7.0 Hz), 2.63 (3H, s), 2.01 (3H, d, J=7.0 Hz). Synthesis Example 47 Starting Material Sodium hydride (0.10 g) was added to a DMF solution (12 ml) of 4-methyl-5-pentafluoroethyl-4H-[1,2,4]triazol-3-thiol (0.70 g), and the mixture was stirred at room temperature until the generation of hydrogen gas stopped. Continuously, 5-fluoro-2-nitrotoluene (0.47 g) was added thereto and the mixture was further stirred at room temperature for 1 hour. After cooling to room temperature, the reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride and then dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained residue was purified by silica gel column chromatography (mixed solvent of n-hexane and ethyl acetate) to obtain the aimed 4-methyl-3-(3-methyl-4-nitrophenyl sulfanyl)-5-pentafluoroethyl-4H-(1,2,4)-triazole (0.55 g). 1 H-NMR (CDCl 3 , ppm): 2.70 (3H, s), 3.80 (3H, s), 8.10-8.30 (3H, m). Synthesis Example 48 Starting Material A mixture of 2-methylmelcapto-4,6-bistrifluoromethyl-pyrimidine (36 g), oxone (126 g), water (500 ml) and chloroform (110 ml) was refluxed for 2 days. After cooling to room temperature, the mixture was extracted with dichloromethane. The obtained organic layer was washed with water and then dried with anhydrous sodium sulfate. After distilling off the solvent, the obtained crude crystals were washed with petroleum ether to obtain 2-methanesulfonyl-4,6-bistrifluoromethyl-pyrimidine (7.5 g). 1 H-NMR (CDCl 3 , ppm): 3.48 (3H, s), 8.19 (1H, s). Synthesis Example 49 Starting Material 4-Nitro-m-cresol (0.77 g), 2-methanesulfonyl-4,6-bistrifluoromethyl-pyrimidine (1.77 g) and potassium carbonate (1.04 g) were refluxed in acetonitrile (15 ml) for 5 hours. After finishing the reaction, the reaction mixture was poured into ice to separate out crystals. The obtained crystals were filtered and dried to obtain 2-(3-methyl-4-nitrophenoxy)-4,6-bistrifluoromethyl-pyrimidine (1.03 g). 1 H-NMR (CDCl 3 , ppm): 2.60 (3H, s), 7.1-7.3 (2H, m), 7.67 (1H, s), 8.10 (1H, d). Synthesis Example 50 Starting Material (3-Methyl-4-nitrophenyl)-acetonitrile (3.52 g) was dissolved in pyridine (30 ml), thereto excess H 2 S was bubbled into at room temperature for 3 hours. Then the mixture was poured onto ice. The precipitate was collected by suction, washed with water and dried to obtain 2-(3-methyl-4-nitro-phenyl)-thioacetamide (1.69 g). 1 H-NMR (CDCl 3 , ppm): 2.60 (3H, s), 4.06 (2H, s), 6.40-8.00 (5H, m) Synthesis Example 51 Starting Material 2-(3-Methyl-4-nitrophenyl)-thioacetamide (1.00 g), 1-bromo-3,3,4,4,4-pentafluoro-2-butanone (1.15 g) and potassium carbonate (0.79 g) were stirred in DMF (10 ml) at room temperature for 1 hour. The reaction solution was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 2-(3-Methyl-4-nitro-phenyl)-thioacetimidic acid 3,3,4,4,4-pentafluoro-2-oxo-butyl ester (1.30 g). 1 H-NMR (CDCl 3 , ppm): 2.55 (3H, s), 3.57 (2H, dd), 3.90 (2H, d), 7.24-7.22 (2H, m), 7.91-7.89 (1H, m) Synthesis Example 52 Starting Material Trifluoroacetic anhydride (1.47 g) was added to 2-(3-Methyl-4-nitro-phenyl)-thioacetimidic acid 3,3,4,4,4-pentafluoro-2-oxo-butyl ester (1.30 g) and triethylamine (0.71 g) in dichloromethane (10 ml), and stirred at room temperature for 20 minutes. The reaction solution was washed with water, and the solvent was distilled off under the reduced pressure and the obtained residue was purified by silica gel column chromatography to obtain 2-(3-methyl-4-nitro-benzyl)-4-perfluoroethyl-thiazole (0.70 g). 1 H-NMR (CDCl 3 , ppm): 2.63 (3H, s), 4.43 (2H, s), 7.30-7.28 (2H, m), 7.75 (1H, s), 7.98 (1H, d) Synthesis Example 53 Starting Material An acetonitrile solution (20 ml) of 3-pentafluoroethyl-1H-pyrazole (2.0 g), dicerium ammonium nitrate (3.0 g) and iodine (1.6 g) was refluxed for 3 hours. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 4-iodo-3-pentafluoroethyl-1H-pyrazole (3.2 g). 1 H-NMR (CDCl 3 , ppm): 7.77 (1H, s), 11.11 (1H, m) Synthesis Example 54 Starting Material 4-Iodo-3-pentafluoroethyl-1H-pyrazole (6.24 g), copper powder (3.81 g), Iodo-1,1,2,2-tetrafluoroethane (9.12 g) and DMF (30 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 120-125° C. After cooling to room temperature, the insoluble material was filtered off through Celite and washed with diethyl ether. The filtrate was diluted with water and extracted with diethyl ether. The organic phase was washed with water and dried over sodium sulfate, and concentrated under the reduced pressure. The crude product was distilled under reduced pressure to obtain 3-pentafluoroethyl-4-(1,1,2,2-tetrafluoroethyl)-1H-pyrazole (0.60 g), bp. 125-135° C./20 mbar. 1 H-NMR (CDCl 3 , ppm): 5.98 (1H, it), 7.96 (1H, s), 12.22 (1H, m) Synthesis Example 55 Starting Material 4-Iodo-3-pentafluoroethyl-1H-pyrazole (12.48 g), copper powder (7.63 g), iodopentafluoroethane (29.50 g) and DMF (60 ml) were set in an autoclave and heated and stirred for 8 hours, maintaining the inside temperature of 120-125° C. After cooling to room temperature, the insoluble material was filtered off through Celite and washed with diethyl ether. The filtrate was diluted with water and extracted with diethyl ether. The organic phase was washed with water and dried over sodium sulfate, and concentrated under the reduced pressure. The crude product was distilled under reduced pressure to obtain 3,4-bis-pentafluoroethyl-1H-pyrazole (1.20 g), bp. 110-115° C./20 mbar. 1 H-NMR (CDCl 3 , ppm): 7.99 (1H, s), 12.31 (1H, m). Synthesis Example 56 Starting Material An acetonitrile solution (20 ml) of 4-methyl-1H-pyrazole (0.5 g), dicerium ammonium nitrate (1.7 g) and iodine (1.9 g) was refluxed for 3 hours. After cooling, the reaction solution was washed with saturated aqueous solution of sodium thiosulfate and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 3,5-diiodo-4-methyl-1H-pyrazole (1.2 g). 1 H-NMR (CDCl 3 , ppm): 2.03 (3H, s), 6.96 (1H, br s) Synthesis Example 57 Starting Material 5-Trifluoromethyl-1H-(1,2,4)-triazole-3-thiol (11.0 g), heptafluoro-1-iodopropane (3.5 g) and triethylamine (0.90 g) were stirred in DMF (10 ml) at 90° C. for 24 hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. After drying the organic layer with magnesium sulfate, the solvent was distilled off under the reduced pressure to obtain 3-heptafluoropropylsulfanyl-5-trifluoromethyl-1H-(1,2,4)-triazole (0.70 g). USE EXAMPLES Biological Test Example 1 Test Against Larva of Spodoptera litura Preparation of Test Solution: Solvent:Dimethylformamide: 3 parts by weightEmulsifier:Polyoxyethylene alkyl phenyl ether: 1 part by weight In order to make an appropriate formulation of an active compound, 1 part by weight of the active compound was mixed with the above-mentioned amount of solvent containing the above-mentioned amount of emulsifier and the mixture was diluted with water to a prescribed concentration. Test Method: Leaves of sweet potato were soaked in the test solution diluted to a prescribed concentration with water, dried in the air and put in a dish of 9 cm diameter. 10 larvae of Spodoptera litura at the third instar were placed on the leaves and kept in a room at the constant temperature of 25° C. After 2 and 4 days further leaves of sweet potato were added and after 7 days the number of dead larvae was counted and the rate of death was calculated. In this test the results of 2 dishes at 1 section were averaged. Biological Test Example 2 Test Against Larva of Cnaphalocrocis medinalis Guenee Test Method: Paddy rice (variety: Tamanishiki) planted in a pot was treated by spraying 50 ml per pot of the diluted aqueous solution of the prescribed concentration of the active compound prepared in the same manner as in the above-mentioned Biological Test Example 1. After the treated rice plant was dried in the air, their foliage part was cut in 4-5 cm length, which were put in a dish with 9 cm diameter with a sheet of filter paper and 2 ml of water. Five larvae of Cnaphalocrocis medinalis Guenee at the second instar were put in the dish that was placed in a room at the constant temperature of 25° C. After 2 and 4 days, each rest (each ⅓ amount) of foliage parts of rice plant were cut in the same manner and added to the dish. After 7 days the number of dead larvae was counted and the rate of death was calculated. In this test the results of 2 dishes at 1 section were averaged. Test Results: In the above Biological Test Examples 1 and 2, as specific examples, the compounds of the aforementioned compound Nos. 8, 9, 10, 11, 12, 13, 14, 15, 16, 45, 47, 48, 49, 51, 52, 53, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 93, 103, 107, 116, 128, 132, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 153, 155, 157, 174, 176, 177, 178, 180, 181, 182, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 221, 222, 226, 227, 229, 230, 231, 238, 239, 242, 243, 251, 253, 262, 264, 268, 270, 281, 299, 308, 310, 318, 322, 413, 414, 417, 422, 434, 446, 448, 473, 475, 492, 506, 508, 512, 518, 520, 539, 543, 544, 545, 546, 547, 548, 549, 552, 554, 559, 561, 562, 563, 564, 565, 566, 567, 568, 570, 571, 572, 573, 574, 578, 579, 580, 626, 637, 638, 639, 640, 641, 642, 643, 644, 645, 646, 647, 648, 649, 650, 655, 656, 657, 658, 659, 660, 661, 662, 663, 664, 665, 666, 667, 668, 669, 670, 671, 672, 681, 761, 762, 763, 804 and 920 showed controlling effect of 100% of rate of death at 20 ppm concentration of the active component. Biological Test Example 3 Test Against Myzus persicae Resistant to Organophosphorous Agents and Carbamates Test Method: About 30 bred Myzus persicae resistant to organophosphorous agents and carbamates were inoculated per 1 seedling of eggplant planted in a vinyl pot of 6 cm diameter. One day after the inoculation, a sufficient amount of a diluted aqueous solution of a prescribed concentration of an active compound prepared as mentioned above, was sprayed by using a spray gun. After spraying it was placed in a green house of 28° C. and the rate of death was calculated 7 days after the spraying. Test was repeated twice. Test Results The compounds of the aforementioned compound Nos. 140, 141, 144, 146, 147, 148, 174, 176, 177, 178, 180, 181, 211, 213, 214, 215, 218, 220, 222, 226, 239, 243, 569, 570, 572, 579, 761, 797 and 920 offered to the test as specific examples showed controlling effect of 100% of rate of death at 100 ppm concentration of the effective component. Formulation Example 1 Granule To a mixture of 10 parts of the compound of the present invention (No. 8), 30 parts of bentonite (montmorillonite), 58 parts of talc and 2 parts of ligninsulfonate salt, 25 parts of water are added, well kneaded, made into granules of 10-40 mesh by an extrusion granulator and dried at 40-50° C. to obtain granules. Formulation Example 2 Granules 95 Parts of clay mineral particles having particle diameter distribution in the range of 0.2-2 mm are put in a rotary mixer. While rotating it, 5 parts of the compound of the present invention (No. 11) are sprayed together with a liquid diluent, wetted uniformly and dried at 40-50° C. to obtain granules. Formulation Example 3 Emulsifiable Concentrate 30 Parts of the compound of the present invention (No. 12), 55 parts of xylene, 8 parts of polyoxyethylene alkyl phenyl ether and 7 parts of calcium alkylbenzenesulfonate are mixed and stirred to obtain an emulsifiable concentrate. Formulation Example 4 Wettable Powder Parts of the compound of the present invention (No. 15), 80 parts of a mixture of white carbon (hydrous amorphous silicon oxide fine powders) and powder clay (1:5), 2 parts of sodium alkylbenzenesulfonate and 3 parts of sodium alkylnaphthalenesulfonate-formalin-condensate are crushed and mixed to make a wettable powder. Formulation Example 5 Water Dispersible Granule Parts of the compound of the present invention (No. 16), 30 parts of sodium ligninsulfonate, 15 parts of bentonite and 35 parts of calcined diatomaceous earth powder are well mixed, added with water, extruded with 0.3 mm screen and dried to obtain water dispersible granules.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}},"description_lang":["en"],"has_description":true,"has_docdb":true,"has_inpadoc":true,"has_full_text":true,"biblio_lang":"en"},"jurisdiction":"US","collections":[],"usersTags":[],"lensId":"177-754-064-321-314","publicationKey":"US_7674807_B2","displayKey":"US 7674807 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wherein\n
X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, C1-4alkylsulfonyloxy, C1-4alkylsulfinyl, C1-4alkylsulfenyl or C1-4alkylsulfonyl,\n
R1 represents C1-4alkyl, C1-4alkylthio-C1-4alkyl, C1-4alkylsulfinyl-C1-4alkyl or C1-4alkylsulfonyl-1-4alkyl,\n
Y represents fluorine, chlorine, bromine or C1-4alkyl,\n
m represents 1,\n
A represents CH2 or CH(CH3), and\n
Q represents a 5-membered or 6-membered heterocyclic group that contains one to three N-atoms and which can be optionally substituted by at least one member selected from a group consisting of C1-6alkyl, C1-6alkoxy, C1-6alkylthio, C1-6alkylsulfinyl, C1-6alkylsulfonyl, C1-6haloalkyl, C1-10haloalkoxy, C1-6haloalkylthio, C1-6haloalkylsulfinyl, C1-6haloalkylsulfonyl, C1-6haloalkylcarbonyl, halogen, oxo and hydroxy."],"number":1,"annotation":false,"title":false,"claim":true},{"lines":["A compound according to claim 1 wherein\n
X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, methanesulfonyloxy, C1-2alkylsulfinyl, C1-2alkylsulfenyl or C1-2alkylsulfonyl,\n
R1 represents isopropyl, C1-2alkylthio-C3-4alkyl, C1-2alkylsulfinyl-C3-4alkyl or C1-2alkylsulfonyl-C3-4alkyl,\n
Y represents fluorine, chlorine or methyl,\n
m represents 1,\n
A represents CH2 or CH(CH3), and\n
Q represents a hetero cyclic group, selected from a group consisting of pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, and pyrimidinyl each of which may be optionally substituted by at least one member selected from the group consisting of C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, C1-8haloalkyl, C1-4haloalkoxy, C1-4haloalkylthio, C1-4haloalkylsulfinyl, C1-4haloalkylsulfonyl, C1-4haloalkylcarbonyl, fluorine, chlorine, bromine, iodine, oxo and hydroxy."],"number":2,"annotation":false,"title":false,"claim":true},{"lines":["A composition comprising a compound according to claim 1 and a diluent or a carrier."],"number":3,"annotation":false,"title":false,"claim":true},{"lines":["A composition according to claim 3, further comprising at least one extender and/or surface active agent."],"number":4,"annotation":false,"title":false,"claim":true},{"lines":["A compound of formula (VIII)\n
wherein\n
X represents hydrogen, halogen, nitro, C1-6alkylsulfonyloxy, C1-6alkylsulfinyl, C1-6alkylsulfenyl or C1-6alkylsulfonyl,\n
Y represents halogen or C1-6alkyl,\n
A represents CH2 or CH(CH3), and\n
Q represents a 5-membered or 6-membered heterocyclic group that contains one to three N-atoms, or one O-atom or one S-atom and can be optionally substituted."],"number":5,"annotation":false,"title":false,"claim":true}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}