WO2005095351A1 - N1 - ((pyrazol-1-ymethyl) -2-methylphenyl)- phatalamide derivatives and related compounds insecticides - Google Patents

N1 - ((pyrazol-1-ymethyl) -2-methylphenyl)- phatalamide derivatives and related compounds insecticides Download PDF

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Publication number
WO2005095351A1
WO2005095351A1 PCT/EP2005/002130 EP2005002130W WO2005095351A1 WO 2005095351 A1 WO2005095351 A1 WO 2005095351A1 EP 2005002130 W EP2005002130 W EP 2005002130W WO 2005095351 A1 WO2005095351 A1 WO 2005095351A1
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formula
methyl
compounds
trifluoromethyl
alkyl
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PCT/EP2005/002130
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French (fr)
Inventor
Katsuaki Wada
Takuya Gomibuchi
Yasushi Yoneta
Yuichi Otsu
Katsuhiko Shibuya
Norihiko Nakakura
Rüdiger Fischer
Tetsuya Murata
Eiichi Shimojo
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Bayer Cropscience Ag
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Priority to DE602005017474T priority Critical patent/DE602005017474D1/en
Priority to JP2007502233A priority patent/JP5336074B2/en
Priority to BRPI0508632-9A priority patent/BRPI0508632A/en
Priority to AU2005229339A priority patent/AU2005229339B2/en
Priority to US10/592,361 priority patent/US7674807B2/en
Priority to AT05731064T priority patent/ATE447556T1/en
Priority to KR1020067021031A priority patent/KR101166122B1/en
Priority to EP05731064A priority patent/EP1727804B1/en
Publication of WO2005095351A1 publication Critical patent/WO2005095351A1/en
Priority to US12/694,441 priority patent/US20100130743A1/en

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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/16—Halogen atoms or nitro radicals
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
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    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D231/08—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with oxygen or sulfur atoms directly attached to ring carbon atoms
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/20—One oxygen atom attached in position 3 or 5
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    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
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    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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    • C07D249/12—Oxygen or sulfur atoms

Definitions

  • the present invention relates to novel benzenedicarboxamides, processes for the preparation thereof, their intermediates and their use as insecticides.
  • X represents hydrogen, halogen atom, nitro, C ⁇ - 6 alkylsulfonyloxy, C-- 6 alkylsulfinyl, Ci- ⁇ alkyl- sulfenyl or C ⁇ . 6 alkylsulfonyl
  • R 1 represents C ⁇ alkyl, C ⁇ . 6 alkylthio-Cj. 6 alkyl, -galkylsulfinyl- - ⁇ alkyl or C ⁇ - 6 alkylsulfo- nyl-C_- 6 alkyl
  • Y represents halogen or C ⁇ - 6 alkyl
  • ⁇ m represents 0 or 1
  • A represents O, S, SO, S0 2 , CH 2 or CH(CH 3 )
  • 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.
  • the compounds of the formula (T), according to the invention can be obtained by (a) reacting compounds of the formula (II)
  • R 1 and X have the same definitions as aforementioned, with compounds of the formula (Dl) 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 ( ) reacting compounds of the formula (IV)
  • R lf represents Ci- ⁇ alkylthio- -galkyl
  • X, Y, A, m and Q have the same definitions as aforementioned, with an oxidizing agent in the presence of inert solvents.
  • the benzenedicarboxamides of the formula (I) show a strong insecticidal action.
  • Halogen represents fluorine, chlorine, bromine and iodine, and preferably represents fluorine, chlorine and bromine.
  • Alkyl represents straight chain or branched chain 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_. 6 alkyl.
  • haloalkyl 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.
  • X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, C M alkylsulfonyloxy, C ⁇ - 4 alkylsulfinyl, C alkylsulfenyl or C M lkylslfonyl
  • R 1 represents C h alky!, C alkylthio-C M alkyl, C al lsulfmyl-C al l or C M alkylsulfo- nyl-C ⁇ --,alkyl,
  • Y represents fluorine, chlorine, bromine or C ⁇ aUcyl.
  • m represents 0 or 1
  • A represents O, S, SO, S0 2 , CH 2 or CH(CH 3 ), and
  • Q 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 h alky!, ⁇ alkoxy, C ⁇ - 6 alkylthio, C ⁇ _ 6 alkylsul- finyl, C ⁇ - 6 alkylsulfonyl, C M0 haloalkyl, - 6 haloalkoxy, C ⁇ - 5 haloalkylthio, Q- ⁇ haloalkylsulf-- nyl, C ⁇ - 6 haloalkylsulfonyl, C ⁇ - 6 haloalkylcarbonyl, halogen, oxo and hydroxy group, can be mentioned as preferable.
  • X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, methanesulfonyloxy, C ⁇ - 2 all ylsulfinyl, C ⁇ - 2 alkylsulfenyl or C ⁇ - 2 alkylslfonyl
  • R 1 represents isopropyl, C ⁇ - 2 alkylthio-C 3 --,alkyl, or C_- 2 alkylsulfo- nyl-C 3 - 4 alkyl
  • Y represents fluorine, chlorine or methyl
  • m represents 0 or 1
  • A represents O, S, SO, S0 2 , CH 2 or CH(CH 3 ), and
  • Q represents heterocyclic group, selected from a group consisting of pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, oxadiazolyl and pyrimidinyl, that can be optional- ly substituted by at least one selected from the group consisting of C ⁇ Ucyl, C lkoxy, C ⁇ - alkylthio, C M alkylsulfinyl .
  • 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-(l,l-dimemyl-2-me ylMoethyli ⁇ nino)-4-iodo-3H-isobenzofuran-l-one and l-(4-amino-3- methylbenzyl)-3,5-bis (trifluoromethyl)-lH-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-l-ylmethyl]-2-methylphenyl ⁇ -4-fluo- roiso ndole- 1,3 -dione and (S)-l-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-(l,l-dimethyl-2-methylthioethyl)-phthalamic acid and 2-methyl-4- [l-(3-trifluoromethylpyrazole-l-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, l-[4-(4-iodo-3-oxo-3H-isobenzofi ⁇ ran-l-ylideneamino)-3-methyI-benzyl]-3,5-bis (trifluoromethyl) ⁇ !, 2,4)-triazol and l-memyl-2-memylthioethylamine 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)-lH-pyrazol-l-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 -(l-me l-2-me lmioe l)-3-iodo-N 1 - ⁇ 2-me l-4-[3,5-bis(trifluoromethyl)-lH-pyra- zol-l-ylmethyl]phenyl ⁇ phthalamide and m-chloroperbenzoic acid are used as starting materials.
  • the compounds of the formula (H), 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • a compound of the formula (EOT) 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.
  • a diluent for example, ethanol
  • the compounds of the formula (HI) can be obtained from the compounds of the formula (IX).
  • 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. ⁇ , p. 254), a process of reacting titanium trichloride under neutral condition, etc.
  • the compounds of the formula (K) are novel compounds and can be obtained by reacting the compounds of the formula (TX) wherein A represents other than oxygen atom, for example, compounds of the formula (X)
  • 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 (XT) H-Q (XI) wherein Q has the same definition as aforementioned.
  • 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 (XT) include known compounds and as their specific examples, there can be mentioned: 3,5-bis (trifluoromethyl)-lH-pyrazole,
  • 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.
  • the diluent used in that case there can be mentioned for example, aliphatic, alicyclic and aromatic hydrocarbons (maybe 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 ket
  • 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-tetramethylethylene- dia ine (TMEDA), N,N-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicy
  • the above-mentioned reaction can also be conducted by a process using a phase transfer catalyst in the presence of a diluent.
  • a 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.
  • DME dimethoxyethane
  • THF tetrahydrofuran
  • DGM diethylene glycol dimethyl ether
  • phase transfer catalyst examples include quaternary ions, for example, tetramethylammonium bromide, tetrapropylammonium bromide, tetrabutylammomum 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.
  • 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 (XT) to 1 mole of the compounds of the formula (X) in a diluent, for example, DMF, in the presence of potassium carbonate.
  • a diluent for example, DMF
  • 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, l-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.
  • 2-(3-methyl-4-rjitrobenzyl)-5-trifluoromethyl-l,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.
  • 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.
  • 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-l,2,4-oxazole can easily be obtained from 3-methyl- 4-nitrobenzamideoxime, according to a method described in J. Qrg. Chem, vol. 68(2), 2003, p. 605-608.
  • 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.
  • 3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-l,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.
  • 2-(3-me l-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.
  • l-methyl-3-(3-memyl-4-mfrophenyl)-5-trifluoromethyl-lH-l,2,4-triazole can easily be prepared by a reaction of the above 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-l,2,4-oxazole with methyl- hydrazine, according to a method described in J. Org. Chem, vol. 68(2), 2003, p.
  • 605 - 608 and also l-methyl-3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-lH-l,2,4-triazole can be done by a reaction of the above 3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-l ,2,4-oxazole with methylhydrazine as well.
  • the compounds of the formula (DC) can be prepared, besides the above-mentioned preparation process, also by the process to be mentioned later in Examples as an alternative.
  • 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 (XIT)
  • the reaction can be conducted in an adequate diluent.
  • a diluent 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
  • 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.
  • 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 (ID) to 1 mole • of the compounds of the formula (X-Q) in a diluent, for example, acetic acid.
  • 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).
  • 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 2045 905, WO 01/23350.
  • ethylamine diethylamine, n-propylamine, isopro- pylamine, n-butylamine, sec-butylamine, isobutylamine, t-butylamine, t-amylamine, 2-(methyl- thio)-ethylamine, 2-(ethylthio)-ethylamine, l-methyl-2-(methylthio)-ethylamine, 1,1-dime- thyl-2-(methylthio)-ethylamine and so on.
  • the compounds of the formula (VT), 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.
  • N-isopropyl-phthalamic acid 3-fluoro-N-isopropyl-phthalamic acid
  • N-(l , 1 -dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid N-(l,l-dimemyl-2-methylsulfanyl-ethyl)-3-fluoro-phthalamic acid,
  • N-isopropyl-3 -methanesulfonyloxy-phthalamic acid N-(l -methyl-2-methylsulfanyl-ethyl)-3-methanesulfonyloxy-phthalamic acid,
  • Xtt The compounds of the above-mentioned formula (Xtt) 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, 0 2-(ethyllMo)ethylamine, l-me yl-2-(memylthio)ethylamine, l,l-dime&yl-2-(memyl1hio)ethylamine, 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, 5 dioxane, dimethoxyethane (DME), tetrahydrofuran (THF), diethylene glycol dimethyl ether (DGM), etc.; ketones, for example, acetone, methyl ethyl ketone
  • 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-diethyl- aniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicyclo[2,2,2]octane (DABCO), l,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.
  • reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure.
  • the aimed compounds of the formula (VT) 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 (XH) in a diluent, for example, acetonitrile.
  • the compounds of the formula ( H), 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 (VIH), 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.
  • the compounds of the formula (NUT), 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 (X ⁇ ) with the compounds of the aforementioned formula (HI).
  • aliphatic, alicyclic and aromatic hydrocarbons may be optionally chlorinated
  • 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
  • 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), ⁇ , ⁇ -dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicyclo[2,2,2]octane (DABCO) and l,8-diazabicyclo[5,4,0]undec-7-ene (DBU), etc.
  • tertiary amines dialkylaminoanilines and pyridines
  • TMEDA 1,1,4,4-tetramethylethylenediamine
  • DMAP 4-dimethylaminopyridine
  • DABCO l,4-diazabicyclo[2,2,2]octane
  • 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.
  • reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure.
  • 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.
  • the compounds of the formula (I), in which the group R ⁇ corresponds to - ⁇ alkylsulfinyl-C ⁇ - 6 alkyl or C ⁇ - 6 alkylsulfonyl-C ⁇ - 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).
  • the reaction of the aforementioned preparation process (a) can be conducted in an adequate diluent singly or mixed.
  • 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.
  • 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.
  • reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure.
  • 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 (IH) to 1 mole of the compounds of the formula ( ⁇ ) in a diluent, for example, 1,2-dichloroethane in the presence of 0.01-0.1 mole amount of p-toluenesulfonic acid.
  • 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.
  • aliphatic, alicyclic and aromatic hydrocarbons may be optionally chlorinated
  • 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,
  • 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.
  • 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.
  • the reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure.
  • 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 reaction of the aforementioned preparation process (f) can be conducted in an adequate diluent.
  • aliphatic, alicyclic and aromatic hydrocarbons may be optionally chlorinated
  • aliphatic, alicyclic and aromatic hydrocarbons may be optionally chlorinated
  • alcohols for example, methanol, ethanol, isopropanol andbutanol
  • acids formic acid, acetic acid, etc.
  • 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.
  • reaction is conducted desirably under normal pressure, it can be operated also under elevated pressure or under reduced pressure.
  • 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.
  • reaction of the aforementioned preparation process (f) can be conducted, for example, according to the process described in JJXKEN 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.
  • the active compounds of the formula (I) of the present invention exhibit exact controlling effect against harmful insects without giving phytotoxicity on cultured plants.
  • 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.
  • Coleoptera pests for example,
  • Lepidoptera pests for example,
  • Lymantria dispar Malacosoma neustria, Pieris rapae, Spodoptera litura, Mamestra brassicae, Chilo suppressalis, Pyrausta nubilalis, Ephestia cautella, Adoxophyes orana, Carpocapsa pomonella,
  • Nephotettix cincticeps Nephotettix cincticeps, Nilaparvata lugens, Pseudococcus comstocki, Unaspis yanonensis, Myzus persicae, Aphis pomi, Aphis gossypii, Rhopalosiphum pseudobrassicas, Stephanitis nashi, Nazara spp., Trialeurodes vaporariorum, Psylla spp.;
  • Tliysanoptera pests for example, Tlirips palmi, Frankliniella occidental;
  • Orthoptera pests for example,
  • Homoptera pests for example,
  • Musca domestica Aedes aegypti, Hylemia platura, Culex pipiens, Anopheles slnensis, Culex tritaeniorliynchus, Liriomyzae trifolii etc.
  • mites there can be mentioned, for example, Tetranychus cinnabarinus, Tetranychus urticae, Panonychus citri, Aculops pelekassi, Tarsonemus spp., etc.
  • nematodes there can be mentioned, for example,
  • novel compounds of the present invention can be effectively used against various harmful animal-parasitic pests (endoparasites and ectoparasites), for example, insects and helminthes.
  • animal-parasitic pests there can be mentioned the following pests:
  • insects there can be mentioned, for example,
  • Gastrophilus spp. Stomoxys spp., Trichodectes spp., Rhodnius spp., Ctenocephalides canis, Cimex lectularius etc.
  • Ornithodoros spp. Ixodes spp., Boophilus spp., etc.
  • insects substances having insecticidal action against pests, which include all of them, are in some cases called as insecticides.
  • 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 can be converted into the customary formulation forms, when they are used as insecticides.
  • 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.
  • 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.
  • 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.
  • organic solvents can also be used as auxiliary solvents.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • crushed and fractionated rocks for example, calcite, marble, pumice, sepiolite, dolomite, etc.
  • synthetic granules of inorganic or organic meals for example, saw dust, coconut shells, maize cobs, tobacco stalks, etc.
  • nonionic and anionic emulsifiers for example, polyoxyethylene fatty acid esters, polyoxyethylene fatty acid alcohol ethers (for example, alkylaryl polyglycol ethers), alkylsulfonates, alkylsulfates, arylsulfonates, etc.
  • Dispersants include, for example, lignin sulfite waste liquor and methyl cellulose.
  • Tackifiers can also be used in formulations (powders, granules, emulsifiable concentrates).
  • 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.
  • inorganic pigments for example, iron oxide, titanium oxide, Prussian Blue, etc.
  • organic dyestuffs such as alizarin dyestuffs, azo dyestuffs or metal phthalocyanine dyestuffs
  • 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.
  • insecticides for example, organophosphorous agents, carbamate agents, carboxylate type chemicals, chlorinated hydrocarbon type chemicals, insecticidal substances produced by microorganisms, etc.
  • 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; ampro- pylfos; ampropylfos-potassium; andoprim; anilazine; azaconazole; azoxystrobin; benalaxyl; benala- xyl-M; benodanil; benomyl; benthiavalicarb-isopropyl; benzamacril; benzamacril-isobutyl; bilanafos; binapacryl; biphenyl; bitertanol; blasticidin-S; boscalid; bromuconazole; bupirimate; buthiobate; butyl- amine; calcium polysulfide; capsimycin; captafol; captan; carbendazi
  • 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
  • Carbamates e.g. alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, azamethiphos, bendiocarb, benfuracarb, bufencarb, butacarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, chloethocarb, 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)
  • 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, di- crotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, epn, ethion, ethoprophos, etrimfos, famphur, fen
  • Pyrethroids e.g. acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-s-cyclopentyl-isomer, bioethanomethiin, biopermethrin, bioresmethrin, cWovaporthrin, cis-cypermethrin, cis-resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, DDT, deltamethrin, empenthrin (lR-isomer), esfenvalerate, etofenprox, fenfluth
  • Chloronicotinyls/neonicotinoids e.g. acetamiprid, clothianidin, dinotefiiran, imidacloprid, niten- pyram, nithiazine, thiacloprid, thiamethoxam
  • Cyclodiene organochlorines e.g. camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor
  • Fiproles e.g. acetoprole, ethiprole, fipronil, vaniliprole
  • Fiproles e.g. acetoprole, ethiprole, fipronil, vaniliprole
  • Mectins e.g. abamectin, avermectin, emamectin, emamectin-benzoate, ivermectin, milbemectin, milbemycin
  • Diacylhydrazines e.g. chromafenozide, halofenozide, methoxyfenozide, tebufenozide
  • Benzoylureas e.g. bistrifluron, chlofluazuron, diflubenzuron, fluazuron, flucycloxuron, flu- fenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron
  • Organotins e.g. azocyclotin, cyhexatin, fenbutatin-oxide
  • Tetronic acid insecticides e.g. spirodiclofen, spiromesifen
  • 16.2 Teframic acid insecticides [e.g. 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-l-azaspiro[4.5]dec-3- en-4-yl ethyl carbonate (alias: carbonic acid, 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-l-azaspiro[4.5]- dec-3-en-4-yl ethyl ester, CAS-Reg.-No.: 382608-10-8) and carbonic acid, cis-3-(2,5-dimethylphe- nyl)-8-methoxy-2-oxo-l-azaspiro[4.5]dec-3-en-4-yl ethyl ester (CAS-Reg.-No.: 203313-25-1)] 17.
  • Carboxamides e.g.
  • Inhibitors of magnesium stimulated ATPase e.g. propargite
  • Phthalamides e.g. N 2 -[l,l-dimemyl-2-(me lsulfonyl)e l]-3-iodo-N 1 -[2-me l-4-[l,2,2,2-tettafluoro-l-(trifluoro- memyl)ethyl]phenyl]-l,2-benzenedicarboxamide (CAS-Reg.-No.: 272451-65-7, flubendiamide))
  • Biologica hormones orpheromones (e.g. azadirachtin, Bacillus spec, Beauveria spec, codlemone, Metarrhizium spec, Paecilomyces spec, thuringiensin, Verticillium spec.)
  • hormones orpheromones e.g. azadirachtin, Bacillus spec, Beauveria spec, codlemone, Metarrhizium spec, Paecilomyces spec, thuringiensin, Verticillium spec.
  • Fumigants e.g. aluminium phosphide, methyl bromide, sulfuryl fluoride
  • a mixture with other known active compounds, such as herbicides, fertilizers, growth regulators, safeners and/or semiochemicals is also possible.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the treatment according to the invention may also result in superadditive (“synergistic") effects.
  • superadditive 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.
  • transgenic plants or plant cultivars 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.
  • 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 defence 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), CryllA, CrylllA, CryIDB2, Cry9c, Cry2Ab, Cry3Bb and CrylF and also combinations thereof) (hereinbelow referred to as "Bt plants").
  • Traits that are also particularly emphasized are the increased defence 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.
  • Bt plants 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).
  • YIELD GARD® for example maize, cotton, soya beans
  • KnockOut® for example maize
  • StarLink® for example maize
  • Bollgard® cotton
  • Nucotn® cotton
  • NewLeaf® potato
  • herbicide-tolerant plants examples include 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), DVH® (tolerance to imidazolinones) and STS® (tolerance to sulphonylureas, for example maize).
  • Herbicide-resistant plants plants bred in a conventional manner for herbicide tolerance
  • Clearfield® for example maize
  • 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.
  • N l - ⁇ 4-[3,5-Bis(1rifluoromethyl)-lH- ⁇ yrazol-l-ylme l]-2-me lphenyl ⁇ -N 2 -(l,l-dimethyl-2-me%l- sulfanylethyl)-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.
  • Trifluoroacetic ar-hydride(1.47g) 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).
  • Emulsifier Polyoxyethylene alkyl phenyl ether : 1 part by weight
  • 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.
  • 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.
  • 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 1/3 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.
  • 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.

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Abstract

Novel benzenedicarboxamides of the formula (I) wherein X represents hydrogen, halogen atom, nitro, C1-6alkylsulfonyloxy, C1-6alkylsulfinyl, C1-6alkylsulfenyl or C1-6alkylsulfonyl, R1 represents C1-6alkyl, C1-6alkylthio-C1-6alkyl, C1-6alkylsulfinyl- C1-6alkyl or C1-6 alkylsulfonyl- C1-6alkyl, Y represents halogen or C1-6alkyl, m represents 0 or 1, A represents O, S, SO, SO2, CH2 or CH(CH3), 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.

Description

Nl- ( (PYRAZOL-l-YMETHYL ) -2 -METHYLPHENYL ) - PHATALAMIDE DERIVATIVES AND RELATED COMPOUNDS INSECTICIDES
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 2001-64268, 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)
Figure imgf000002_0001
wherein X represents hydrogen, halogen atom, nitro, Cι-6alkylsulfonyloxy, C--6alkylsulfinyl, Ci-βalkyl- sulfenyl or Cι.6alkylsulfonyl, R1 represents C^alkyl, Cι.6alkylthio-Cj.6alkyl, -galkylsulfinyl- -βalkyl or Cι-6 alkylsulfo- nyl-C_-6alkyl, Y represents halogen or Cι-6alkyl,
■ m represents 0 or 1, A represents O, S, SO, S02, CH2 or CH(CH3), 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.
The compounds of the formula (T), according to the invention, can be obtained by (a) reacting compounds of the formula (II)
Figure imgf000002_0002
wherein R1 and X have the same definitions as aforementioned, with compounds of the formula (Dl)
Figure imgf000003_0001
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 ( ) reacting compounds of the formula (IV)
Figure imgf000003_0002
wherein X, Y, A, m and Q have the same definitions as aforementioned, with compounds of the formula (V) H2N-R1 (V) wherem R1 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)
Figure imgf000003_0003
wherein X and R1 have the same definitions as aforementioned, with the compounds of the formula (III),
Figure imgf000003_0004
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 ( reacting compounds of the formula (VII)
Figure imgf000003_0005
wherein X, Y, A, m and Q have the same definitions as aforementioned, with the compounds of the formula (V), H2N-R1 (V) wherein R1 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 (VDI)
Figure imgf000004_0001
wherein X, Y, A, m and Q have the same definitions as aforementioned, are reacted with the compounds of the formula (V), H2N-R1 (V) wherein R1 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 R1 represents C].6alkylsulfinyl-Cι-6alkyl or Cι-fialkylsulfonyl-Cj-6alkyl in the formula (I), reacting compounds of the formula (If)
Figure imgf000004_0002
wherein Rlf represents Ci-βalkylthio- -galkyl, and X, 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 (f) 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
Figure imgf000005_0001
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_.6alkyl.
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, CM alkylsulfonyloxy, Cι-4alkylsulfinyl, C alkylsulfenyl or CM lkylslfonyl, R1 represents Chalky!, C alkylthio-CMalkyl, C al lsulfmyl-C al l or CMalkylsulfo- nyl-Cι--,alkyl,
Y represents fluorine, chlorine, bromine or C^aUcyl. m represents 0 or 1,
A represents O, S, SO, S02, CH2 or CH(CH3), and
Q 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 Chalky!, ^alkoxy, Cι-6alkylthio, Cι_6alkylsul- finyl, Cι-6alkylsulfonyl, CM0haloalkyl, -6 haloalkoxy, Cι-5haloalkylthio, Q-βhaloalkylsulf-- nyl, Cι-6haloalkylsulfonyl, Cι-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, Cι-2all ylsulfinyl, Cι-2 alkylsulfenyl or Cι-2alkylslfonyl, R1 represents isopropyl, Cι-2alkylthio-C3--,alkyl,
Figure imgf000006_0001
or C_-2alkylsulfo- nyl-C3-4alkyl, Y represents fluorine, chlorine or methyl, m represents 0 or 1,
A represents O, S, SO, S02, CH2 or CH(CH3), and
Q represents heterocyclic group, selected from a group consisting of pyrazolyl, triazolyl, pyrazolinyl, imidazolyl, thiazolyl, pyrrolyl, oxadiazolyl and pyrimidinyl, that can be optional- ly substituted by at least one selected from the group consisting of C^ Ucyl, C lkoxy, Cι- alkylthio, CMalkylsulfinyl. ClJ(alkylsulfonyl5 Cι-8haloalkyl, C_-4haloalkoxy, -^aloal- kylthio, Cι-4haloalkylsulfinyl, CMhaloalkylsulfonyl, CMhaloalkylcarbonyl, 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 R1 has an asymmetric carbon.
The aforementioned process (a) can be illustrated by the following reaction scheme in case that, for example, 3-(l,l-dimemyl-2-me ylMoethyliιnino)-4-iodo-3H-isobenzofuran-l-one and l-(4-amino-3- methylbenzyl)-3,5-bis (trifluoromethyl)-lH-pyrazole are used as starting materials.
Figure imgf000006_0002
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-l-ylmethyl]-2-methylphenyl}-4-fluo- roiso ndole- 1,3 -dione and (S)-l-methyl-2-methylthioethylamine are used as starting materials.
Figure imgf000007_0001
The aforementioned preparation process (c) can be illustrated by the following reaction scheme in case that, for example, 3-iodo-N-(l,l-dimethyl-2-methylthioethyl)-phthalamic acid and 2-methyl-4- [l-(3-trifluoromethylpyrazole-l-yl)-ethyl]-aniline are used as starting materials.
Figure imgf000007_0002
The aforementioned preparation process (d) can be illustrated by the following reaction scheme in case that, for example, l-[4-(4-iodo-3-oxo-3H-isobenzofiιran-l-ylideneamino)-3-methyI-benzyl]-3,5-bis (trifluoromethyl)^!, 2,4)-triazol and l-memyl-2-memylthioethylamine are used as starting materials.
Figure imgf000007_0003
The aforementioned preparation process (e) can be illustrated by the following reaction scheme in case that, for example, N-{4-[3,5-bis (trifluoromethyl)-lH-pyrazol-l-ylmethyl]-2-methyl-phenyl}-6-iodo- phthalamic acid and 1 -methyl-2-methylthioethylamine are used as starting materials. + acid binder
Figure imgf000008_0001
The aforementioned process (f) can be illustrated by the following reaction scheme in case that, for example, N2-(l-me l-2-me lmioe l)-3-iodo-N1-{2-me l-4-[3,5-bis(trifluoromethyl)-lH-pyra- zol-l-ylmethyl]phenyl}phthalamide and m-chloroperbenzoic acid are used as starting materials.
Figure imgf000008_0003
The compounds of the formula (H), 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 (TO), used as starting materials in the preparation process (a), there can be mentioned the following:
3-isopropylimino-3H-isobenzofuran-l-one, 4-fluoro-3-isopropylimino-3H-isobenzofuran-l -one,
4-chloro-3-isopropylimino-3H-isobenzofuran-l-one,
4-bromo-3 -isopropylimino-3H-isobenzofuran- 1 -one,
4-iodo-3-isopropylimino-3H-isobenzofuran-l-one,
3-(l -methyl-2-memylsulfanyl-e1hylimino)-3H-isobenzofuran-l -one, 4-fluoro-3-(l-me yl-2-methylsulfanyl-ethylirmno)-3H-isobenzofuran-l-one,
4-cWoro-3-(l-memyl-2-methylsulfanyl-e1hylimino)-3H-isobenzofuran-l-one5
4-bromo-3-(l-memyl-2-memylsulfanyl-e1hylimino)-3H-isobenzofur--n-l-one,
4-iodo-3-(l-methyl-2-methylsulfanyl-ethylimino)-3H-isobenzofuran-l-one,
3-(l,l-dimemyl-2-methylsulfanyl-ethylirnino)-3H-isobenzofuran-l-one, 3-(l,l-dimethyl-2-memylsulfanyl-e1hylimino)-4-fluoro-3H-isobeι-zoft-ran-l-one, 4-chloro-3 -(1,1 -dimethyl-2-memylsulfanyl-e1hylimino)-3H-isobenzofuran-l -one, 4-bromo-3-(l,l-dimemyl-2-memylsulfanyl-ethylimino)-3H-isobenzofuran-l-one, 3 -( 1 , 1 -dimelhyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-l -one, 3-isopropylimino-l -oxo-1 ,3-dihydro-isobenzofuran-4-yl methanesulfonate 3-(l-methyl-2-memylsulfanyl-ethylmrin^
3-(l,l-dimemyl-2-memylsulfanyl-ethylimino)-l-oxo-l,3-dihydro-isobenzofuran-4-yl methanesulfonate and so on.
The compounds of the formula (UJ), 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)
Figure imgf000009_0001
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 (EOT) 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 (HI) 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. π, p. 254), a process of reacting titanium trichloride under neutral condition, etc.
The compounds of the formula (K) are novel compounds and can be obtained by reacting the compounds of the formula (TX) wherein A represents other than oxygen atom, for example, compounds of the formula (X)
Figure imgf000010_0001
wherein
Y and m have the same definitions as aforementioned, A1 represents S, SO, SO2, CH2 or CH(CH3), and M represents chlorine, bromine or methanesulfonyloxy, with compounds of the formula (XT) H-Q (XI) wherein Q has the same definition as aforementioned.
The compounds of the formula (X), are 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. I l l (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 chloride
4-nitrobenzyl methanesulfonate
2-methyl-4-nitrobenzyl methanesulfonate 3-methyl-4-nitrobenzyl methanesulfonate,
4-nitrobenzenesulfenyl chloride,
4-nitrobenzenesulfinyl chloride,
4-nitrobenzenesuIfonyl chloride,
4-nitro-3 -methylbenzenesulfonyl chloride, 3 -fluoro-4-nitrobenzyl bromide, 3-chloro-4-r-itrobenzyl 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 (XT) include known compounds and as their specific examples, there can be mentioned: 3,5-bis (trifluoromethyl)-lH-pyrazole,
5-difluoromethoxy-3-trifluoromethyl-lH-pyrazole,
4-pentafluoroethyl-lH-ρyrazole,
5-hexafluoro-n-propyl-lH-pyrazole,
3,5-bis (trifluoromethyl)-lH-(l,2,4)-triazole, 5 -pentafluoroethyl-3 -trifluoromethyl- 1 H-(l ,2,4)-triazole,
5-difluoromethyl-3-trifluoromethyl-lH- (1 ,2,4)-triazole,
5-hydroxy-3,5-bis (trifluoromethyl)-lH-4,5-dihydropyrazole,
2,4-bis (trifluoromethyl)-lH-imidazole,
3-(2,2,2-trifluoroe l)-5- trifluoromethyl-l, 2-dihydro-(l,3,4)-triazol-2-one, 2,5-bis (trifluoromethyl)-(l,3,4)-triazole,
5-pentafluoroethyl-lH-pyrazole,
3-pentafluoroethyl-lH-pyrazole,
4-bromo-3-trifluoromethyl-lH-pyrazole,
3-trifluoromethyl-lH-pyrazole, 5-(difluoromethyl)-l,2-dihydro-2-methyl-3H-(l,2,4)-triazol-3-one,
4-(trifluoromethyl)-2H-l,2,3-triazole,
4-iodo-3- pentafluoroethyl-lH-pyrazole,
3-pentafluoroethyl-4-(l,l,2,2-tetrafluoroethyl)-lH-pyrazole,
3,4-bis-pentafluoroethyl-lH-pyrazole, 3,5-diiodo-4-methyl-lH-pyrazole,
3-Heptafluoropropylsulfanyl-5-trifluoromethyl-lH-(l,2,4)-triazole,
3,5-bis(pentafluoroethyl)-lH-(l,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 (maybe 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, l,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-tetramethylethylene- dia ine (TMEDA), N,N-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicyclo[2,2,2]octane (DABCO), l,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, tetrabutylammomum 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 (XT) 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 (HI) mentioned hereinafter. And, as one typical example, l-(3-memyl-4-nifrobenzyl)-3,5-bis-(trifluoromethyl)-lH-pyrazole can be mentioned.
Furthermore, in a case where Q represents 2-thiazolyl in the formula (DC), 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, l-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 l,3,4-oxadiazol-2-yl in the formula (IX), as a specific example, 2-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-l,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-rjitrobenzyl)-5-trifluoromethyl-l,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-l,2,3-triazol-2-yl in the formula (IX), as a specific example, 2-(3-memyl-4-nifrobenzyl)-2H-4-trifluoromethyl-l,2,3-triazole can easily be prepared by a reaction of a known 3-methyl-4-nitrobenzyl chloride with a known 2H-4-trifluoromethyl-l,2,3-triazole described in J. Chem. Soc, Perkin Transaction 2, vol. 10 (1989) p. 1355 to 1375. In a case where Q represents lH-l,2,4-triazol-l-yl in the formula ( C), as a specific example, 5-(3-memyl-4-nifrophenylsulf-fflyl)-l-methyl-3-trifluoromethyl-lH-l,2,4-triazole can easily be prepared by a reaction of l-fluoro-3-methyl-4-nitrobenzene with a known 5-mercapto-l-methyl-3-trifluoro- methyl-lH-l,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 l,2,4-oxazol-3-yl in the formula (IX), as a specific example, 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-l,2,4-oxazole can easily be obtained from 3-methyl- 4-nitrobenzamideoxime, according to a method described in J. Qrg. 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-l,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-me l-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.
hi a case where Q represents lH-l,2,4-triazol-3-yl in the formula (IX), as specific examples, l-methyl-3-(3-memyl-4-mfrophenyl)-5-trifluoromethyl-lH-l,2,4-triazole can easily be prepared by a reaction of the above 3-(3-methyl-4-nitrophenyl)-5-trifluoromethyl-l,2,4-oxazole with methyl- hydrazine, according to a method described in J. Org. Chem, vol. 68(2), 2003, p. 605 - 608, and also l-methyl-3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-lH-l,2,4-triazole can be done by a reaction of the above 3-(3-methyl-4-nitrobenzyl)-5-trifluoromethyl-l ,2,4-oxazole with methylhydrazine as well.
The compounds of the formula (DC) 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 (IU) there can be mentioned, for example, the following:
1 -(4-amino-3 -methylbenzyl)-3,5-bis (trifluoromethyl)- 1 H-pyrazole, l-(4-amino-3-methylbenzyl)-5-difluoromethoxy-3-trifluoromethyl-lH-pyrazole, l-(4-amino-3-methylbenzyl)-4-pentafluoroethyl-lH-pyrazole, l-(4-amino-3-methylbenzyl)-5-hexafluoro-n-propyl-lH-pyrazole, l-(4-arrano-3-methylbenzyl)-3,5-bis (trifluoromethyl)-lH-(l,2,4)-triazole, l-(4-amino-3-methylbenzyl)-5-pentafluoroethyl-3-trifluoromethyl-lH-(l,2,4)-triazole, l-(4-amino-3-memylbenzyl)-5-difluoromemyl-3- trifluoromethyl-lH-(l,2,4)-triazole,
4-(4-amino-3-memylbenzyl)-5-difluoromethoxy-l-difluoromethyl-3-trifluoromethyl-lH-pyrazole,
4-(4-aιruno-3-me&ylbenzyl)-3-difluoromemoxy-l-difluoromemyl-5-trifluoromethyl-lH-pyrazole, l-(4-amino-3-methylbenzyl)-5-hydroxy-3, 5-bis (trifluoromethyl)-lH-4,5-dihydropyrazole, l-(4-amino-3-methylbenzyl)-2,4-bis (trifluoromethyl)-lH-imidazole,
4-(4-ammo-3-me lbenzyl)-2-(2,2,2-1rifluoroethyl)-5-trifluoromethyl-2,4-dihydro-3H-(l,2,4)-t^
-3 -one,
2-(4-ammo-3-me lbenzyl)-4-(2,2,2-trifluoroethyl)-5-trifluorome l-2,4-dihydro-3H-(l,2,4)-t^ azol-3-one, l-(4-amino-3-methylbenzyl)-2,5-bis (trifluoromethyl)-l,3,4-triazole,
2-(4-amino-3 -methylbenzyl)-4,6-bis (trifluoromemyl)-pyrimidine,
2-(4-amino-3 -methylphenoxy)-4,6-bis (trifluoromethyl)-ρyrimidine, l-(4-amino-3-methylphenyl)-3,5-bis (trifluoromethyl)-lH-pyrazole, l-(4-amino-3-methylphenyl)-5-pentafluoroethyl-lH-pyrazole, 1 -(4-amino-3 -methylρhenyl)-3 -pentafluoroethyl-1 H-pyrazole, l-(4-amino-3-methylphenyl)-4-pentafluoroethyl-lH-pyrazole, l-(4-amino-3-methylphenyl)-3-methyl-5-trifluoromethyl-lH-ρyrazole,
1 -(4-amino-3 -methylphenyl)-5 -methyl-3 -trifluoromethyl- 1 H-pyrazole, l-(4-amino-3-methylphenyl)-3-pentafluoroethyl-5-trifluoromethyl-lH-pyrazole, l-(4-amino-3-methylphenyl)-4-bromo-3-trifluoromethyl-lH-pyrazole, l-(4-amino-3-methylphenyl)-3-trifluoromethyl-lH-pyrazole, l-(4-aιnino-3-memylphenyl)-5-hydroxy-3-(2,2,2-1rifluoroe1hyl)-5-trifluoromemyl-lH-4,5-dihydro- pyrazole,
5-(4-armno-3-memylphenyl)-l-(2,2,2-1rifluoroethyl)-3-trifluoromethyl-pyrazole, 5-(4-aιr no-3-memylphenyl)-l-difluoromethyl-3-trifluoromethyl-pyrazole,
3-(4-amino-3-methylphenyl)-l-difluoromethyl-3-difluoromethoxy-pyrazole,
1 -(4-amino-3-methylbenzyl)-3,4-bis (pentafluoroethyl)-lH-pyrazole, l-(4-arnino-3-methylbenzyl)-3,5-bis (pentafluoroethyl)-lH-pyrazole, l-(4-amino-3-methylbenzyl)-3,4-bis (pentafluoroρropyl)-lH-pyrazole, l-(4-amino-3-methylbenzyl)-3,5-bis (pentafluoropropyl)-l H-pyrazole, l-(4-arnino-3-methylbenzyl)-3,5-bis (pentafluoroethyl)-lH-(l,2,4)-triazole, l-(4-aιιιino-3-memylbenzyl)-2,5-bis (pentafluoroethyl)-lH-(l,3,4)-triazole,
2-(4-amino-3-methylphenyl)-5-(trifluoromethyl)-l,3,4-oxadiazole,
2-(4-amino-3-methylphenyl)-5-(pentafluoroethyl)-l,3,4-oxadiazole, 2-(4-anino-3-methylphenyl)-5-(heptafluoropropyl)-l,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-aιmno-3-me1hylphenyl)sulfanyl-l-memyl-3-(trifluoromethyl)-lH-l,2,4-triazole, 3-(4-amino-3-methylphenyl)- 5-(trifluoromethyl)-l,2,4-oxadiazole, 3-(4-amino-3-memylphenyl)-l-methyl-5-(trifluoromethyl)-lH-l,2,4-triazole, l-(4-amino-3-chlorobenzyl)-3,5-bis (trifluoromethyl)-lH-pyrazole, l-(4-ammo-3-fluorobenzyl)-3,5-bis (trifluoromethyl)-lH-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 (XIT)
Figure imgf000016_0001
wherein X has the same definition as aforementioned, with the compounds of the formula (IU).
Figure imgf000016_0002
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 men- tioned, 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, l,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 (ID) to 1 mole • of the compounds of the formula (X-Q) in a diluent, for example, acetic acid.
Many of the compounds of the above-mentioned formula (XH) are publicly known, and as their specific examples there can be mentioned, phthalic anhydride, 3-fluorophthalic anhydride, 3-chloro- phthalic anhydride, 3-bromophthalic anhydride, 3-iodophthalic anhydride, 3-methanesulfonyloxy- phthalic 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-cWoro-2-{2-memyl-4-[3,5-bis(trifluoromemyl)-lH-pyrazol-l-ylmemyl]phenyl}-isoindole-l,3-dione, 2-{2-methyl-4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl-methyl]-phenyl}-isoindole-l,3-dione, 4-chloro-2-[2-memyM-(5-difluoromethoxy-3-trifluoromethyl-lH-pyrazol-l-yl-methyl)-phenyl]-iso- indole-l,3-dione, 4-chloro-2-[2-methyl-4-(4-pentafluoroethyl- lH-pyrazol- 1 -yl-methyl)-phenyl]-isoindole- 1 ,3 -dione, 4-bromo-2-{2-methyl-4-[3,5-bis(trifluoromemyl)-lH-pyrazol-l-yl-methyl]-phenyl}-isoindole-l,3-dione, 4-bromo-2-[2-memyl-4-(5-difluoromethoxy-3-trifluoromethyl-lH-pyrazol-l-yl-methyl)-phenyl]-iso- indole-l,3-dione, 4-bromo-2-[2-methyl-4-(4-ρentafluoroethyl-lH-pyrazol-l-yl-methyl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-{2-memyl-4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl-methyl]-phenyl}-isoindole-l,3-dione, 4-iodo-2-[2-memy]-4-(5-difluoromethoxy-3-trifluoromethyl-lH-pyrazol-l-yl-methyl)-phenyl]-iso- indole-l,3-dione, 4-iodo-2-[2-methyl-4-(4-pentafluoroethyl-lH-pyrazol-l-yl-methyl)-phenyl-]isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(5-hexafluoro-n-propyl-lH-pyrazol-l-yl-methyl)-phenyl]-isoindole-l,3-dione, 4-memanesulfonyloxy-2-{2-methyl-4-[3,5-bis(1rifluoromethyl)-lH-pyrazol-l-yl-methyl]-phenyl}- isoindole- 1 ,3 -dione, 4-chloro-2- {2-methyl-4-[3,5 -bis(trifluoromethyl)- lH-( 1 ,2,4)-triazol- 1 -yl-methyl]-phenyl} -isoindole- 1,3-dione, 4-cMoro-2-{2-me l-4-[5-peatafluoroe l-3-trifl 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-memyl-4-[3,5-bis(trifluoromemyl)-lH-(l,2,4)-1riazol-l-yl-me1hyl]-phenyl}-isoindole-l,3- dione,
4-iodo-2-{2-memyl-4-[5-pentafluoroethyl-3-trifluoromefcyl-lH-(l,2,4)-triazol-l-yl-methyl]-phenyl}- isoindole-1 ,3-dione,
4-iodo-2-{2-memyl-4-[5-difluoromethyl-3-trifluorome l-lH-(l,2,4)-triazol-l-yl-methyl]-phenyl}- isoindole-1, 3 -dione,
4-mem-mesulfonyloxy-2-{2-memyl-4-[3,5-bis(1rifluoromemyl)-lH-(l,2,4)-triazol-l-yl-methyl]-phenyl}
-isoindole- 1 ,3 -dione,
4-iodo-2-[2-memyl-4-(5-difluoromemoxy-l-difluoromemyl-3-1rifluoromethyl-lH-pyrazol-4-yl-methyl)
-phenyl]-isoindole-l ,3-dione, 4-iodo-2-[2-methyl-4-(5-hydroxy-3,5-bis(trifluoromethyl)-lH-4,5-dihydropyrazol-l -yl-methyl)-phe- nyl]-isoindole-l,3-dione,
4-iodo-2-{2-memyM-[2,4-bis(trifluoromemyl)-lH-imidazol-l-yl-methyl]-ρhenyl}-isoindole-l,3-dione,
4-iodo-2-{2-me l-4-[3-(2,2,2-trifluoroe l)-5-1rifl^ methyl]-phenyl} -isoindole-1 ,3-dione, 4-iodo-2-{2-mefl-y^ methyl]-phenyl} -isoindole- 1 ,3-dione,
4-iodo-2-{2-memyl-4-[2,5-bis(trifluoromemyl)-(l,3,4)-triazol-l-yl-methyl]-ρhenyl}-isoindole-l,3-dione,
4-iodo-2-{2-memyl-4-[4,6-bis(trifluoromemyl)pyrimddm-2-yl-memyl]-phenyl}-isoindole-l,3-dione,
4-iodo-2-{2-memyl-4-[4,6-bis(trifluoromemyl)ρyri]τudin-2-yloxy]-phenyl}-isoindole-l,3-dto^ 4-cWoro-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl]-phenyl}-isoindole-l,3-dione,
4-chloro-2-[2-methyl-4-(5-pentafluoroethyl- lH-pyrazol- 1 -yl)-ρhenyl]-isoindole- 1 ,3 -dione,
4-chloro-2-[2-methyl-4-(3-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione,
4-c oro-2-[2-memyl-4-(4-penlBfluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione,
4-iodo-2-[2-memyl-4-[3-methyl-5-trifluoromethyl-lH-pyrazol-l-yl]-phenyl]-isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(5-methyl-3-trifluoromethyl- lH-pyrazol- 1 -yl)-phenyl]-isoindole- 1 ,3 -dione,
4-iodo-2-[2-memyl-4-(3-pentafluoroethyI-5-trifluoromemyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3- dione,
4-iodo-2-[2-methyl-4-(4-bromo-3-trifluoromethyl-lH-pyrazol-l-yl)phenyl]isoindole-l,3-dione,
4-iodo-2-[2-methyl-4-(3-trifluoromethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-{2-me l-4-[5-hydroxy-3-(2,2,2-trifluoroe l)-5-trifluorome l-lH-4,5-dihydropyr-β^ yl]-phenyl} -isoindole-1 ,3-dione, 4-iodo-2-{2-methyl-4-[l-(2,2,2-1rifluoroe l)-3-trifluoromemyl-ρyrazol-5-yl]-ρhenyl}-isoindole-l,3^ dione,
4-iodo-2-[2-methyl-4-(l-difluoromemyl-3-trifluorome yl-pyrazol-5-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(l-(hfluoromethyl-3-difluoromethoxy-pyrazol-3-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-{2-methyl-4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl]-phenyl}-isoindole-l,3-dione, 4-iodo-2-[2-methyl- -(5-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(3-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(4-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-bromo-2- {2-methyl-4-[3,5-bis(trifluoromethyl)- lH-pyrazol- 1 -yl]-phenyl} -isoindole- 1 ,3-dione, 4-bromo-2-[2-methyl-4-(5-pentafluoroethyI- lH-pyrazol- 1 -yl)-phenyI-isoindole- 1 ,3-dione, 4-bromo-2-[2-methyl-4-(3-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-bromo-2-[2-methyl-4-(4-pentafluoroethyl-lH-pyrazol-l-yl)-phenyl]-isoindole-l,3-dione, 4-cMoro-2-{2-me yl-4-[3,4-bis entafluoroethyl)-lH-pyrazol-l-ylmemyl]-phenyl}-isoindole-l,3-dione, 4-cWoro-2-{2-memyl-4-[3,5-bis(pentafluoroethyl)-lH-pyrazol-l-ylmemyl]-phenyl}-isoindole-l,3-dione, 4-cHoro-2-{2-methyl^-[3,4-bis(heptafluoropropyl)-lH-pyrazol-l-ylmethyl]-phenyl}-isoindole-l,3- dione,
4-cMoro-2-{2-memyM-[3,5-bis(h tafluoropropyl)-lH-pyrazol-l-ylmethyl]-phenyl}-isoindole-l,3- dione, 4-chloro-2-[2-methyl-4-(5-trifluoromethyl-l,3,4-oxadiazol-2-yl)-phenyl]-isoindole-l,3-dione, 4-chloro-2-[2-methyl-4-(5-pentafluoroethyl-l,3,4-oxadiazol-2-yl)-phenyl]-isoindole-l,3-dione, 4-chloro-2-[2-methyl-4-(5-heptafluoropropyl-l,3,4-oxadiazol-2-yl)-phenyl]-isoindole-l,3-dione, 4-chloro-2-[2-memyl-4-(5-trifluoromethyl-l,3,4-oxadiazol-2-yl-methyl)-phenyl]-isoindole-l,3-dione, 4-cHoro-2-[2-memyl-4-(4-trifluoromemyl-2H-l,2,3-triazol-2-yl-methyl)-phenyl]-isoindole-l,3-dione, 4-cWoro-2-[2-methyl-4-(4-(pentafluoroethyl)-thiazol-2-yl-methyl)-phenyl]-isoindole-l,3-dione, 4-chloro-2-{2-methyl-4-[l-methyl-3-(trifluoromethyl)-lH-l,2,4-triazol-5-yl-sufanyl]-phenyl}-iso- indole- 1,3 -dione,
4-cUoro-2-[2-methyl-4-(5-trifluoromethyl-l,2,4-oxadiazol-3-yl)-phenyl]-isoindole-l,3-dione, 4-cWpro-2-[2-memyl-4-(l-memyl-5-trifluoromemyl-lH-l,2,4-triazol-3-yl)-phenyl]-isoindole-l,3-dione, 4-iodo-2-[2-methyl-4-(5-trifluoromethyl-l,3,4-oxadiazol-2-yl)-phenyl]-isoindole-l,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 2045 905, WO 01/23350.
As their specific examples there can be mentioned ethylamine, diethylamine, n-propylamine, isopro- pylamine, n-butylamine, sec-butylamine, isobutylamine, t-butylamine, t-amylamine, 2-(methyl- thio)-ethylamine, 2-(ethylthio)-ethylamine, l-methyl-2-(methylthio)-ethylamine, 1,1-dime- thyl-2-(methylthio)-ethylamine and so on.
The compounds of the formula (VT), 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-(l-methyl-2-methylsulfanyl-ethyl)-ρhthalamic acid, 3-fluoro-N-(l-methyl-2-methylsulfanyl-ethyl)-ρhthalamic acid,
3-chloro-N-(l-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,
3-bromo-N-(l-methyl-2-methylsulfanyl-ethyl)-phthalamic acid,
3-iodo-N-(l -methyl-2-methylsulfanyl-ethyl)-phthalamic acid,
N-(l , 1 -dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid, N-(l,l-dimemyl-2-methylsulfanyl-ethyl)-3-fluoro-phthalamic acid,
3 -chloro-N-(l , 1 -dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid,
3-bromo-N-(l , 1 -dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid,
N-(l , 1 -dimethyl-2-memylsulfanyl-ethyl)-3-iodo-phthalamic acid,
N-isopropyl-3 -methanesulfonyloxy-phthalamic acid, N-(l -methyl-2-methylsulfanyl-ethyl)-3-methanesulfonyloxy-phthalamic acid,
N-( 1 -methyl-2-methylsulfanyl-ethyl)-3 -nitro-phthalamic acid,
3-chloro-N-(2-ethylsulfanyl-l-methyl-ethyl)-phthalamic acid,
3-bromo-N-(2-ethylsulfanyl-l -methyl-ethyl)-phthalamic acid,
N-(2-ethylsulfanyl-l -methyl-ethyl)-3-iodo-phthalamic acid, N-(2-ethylsulfanyl-l-methyl-ethyl)-3-nitro-phthalamic acid,
N-(2-ethylsulfanyl- -methyl-ethyl)-3-methanesulfonyloxy-phthalamic acid,
N-(l,l-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 (XH)
Figure imgf000021_0001
wherein X has the same definition as aforementioned, with amines of the formula H2N-R1 pan)
5 wherein R! has the same definitions as aforementioned,
The compounds of the above-mentioned formula (Xtt) 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, 0 2-(ethyllMo)ethylamine, l-me yl-2-(memylthio)ethylamine, l,l-dime&yl-2-(memyl1hio)ethylamine, etc.
These amines can be easily obtained also by the process described in DE-A 2045 905, WO 01/23350, etc. [5 The above-mentioned reaction of the compounds of the formula (XH) with the amines of the formula (Xπi) can be conducted according to the process described in, for example, J. Org. Chem, Vol.46, p. 175 (1981) etc. 0 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, 5 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. 0 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-diethyl- aniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicyclo[2,2,2]octane (DABCO), l,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 (VT) 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 (XH) in a diluent, for example, acetonitrile.
The compounds of the formula ( H), 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 (VIH), 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 (VH), there can be mentioned the following: l-[4-(4-iodo-3-oxo-3H-isobenzoftιran-l-ylideneamino)-3-methyl-benzyl]-3,5- bis(trifluoromethyl)-lH-pyrazole, l-[4-(4-cWoro-3-oxo-3H-isobenzofuran-l-ylideneamino)-3-methyl-benzyl]-3,5- bis(trifluoromethyl)-lH-pyrazole, l-[4-(4-iodo-3-oxo-3H-isobeιιzofiu-an-l-ylideneamino)-3-methyl-benzyl]-3,5- bis(trifluoromethyl)-l ,2,4-triazole, l-[4-(4-iodo-3-oxo-3H-isobenzofύran-l-ylideneamino)-3-methylphenyl]-3,5- bis(trifluoromethyl)-lH-pyrazole, l-[4-(4-cUoro-3-oxo-3H-isobenzoftιran-l-ylideneamino)-3-methyl-benzyl]-3,4- bis(pentafluoroethyl)-lH-pyrazole, l-[4-(4-cWoro-3-oxo-3H-isober-zofuran-l-ylideneamino)-3-methyl-benzyl]-3,5- bis(pentafluoroethyl)-lH-pyrazole, l-[4-(4-cWoro-3-oxo-3H-isobenzofuran-l-ylideneaιr_ino)-3-methyl-benzyl]-3,4- bis(heptafluoropropyl)-lH-pyrazole, l-[4-(4-chioro-3-oxo-3H-isoberι-zofuran-l-ylideneamino)-3-methyl-benzyl]-3,5- bis(heptafluoropropyl)-lH-pyrazole,
2-[4-(4-chloro-3-oxo-3H-isobenzofi-ran-l-ylideneaιr-ino)-3-methylphenyl]-5-(trifluoromethyl)-l,3,4- oxadiazole,
2-[4-(4-chloro-3-oxo-3H-isoberιzofuran-l-ylideneaιrιino)-3-memylphenyl]-5-(pentafluoroethyl)-l,3,4
-oxadiazole, 2-[4-(4-chloro-3-oxo-3H-isobenzofuran-l-ylideneamino)-3-methylphenyl]-5-(heptafluoropropyl)-l,3,
4-oxadiazole,
2-[4-(4-cUoro-3-oxo-3H-isobenzofiπ-an-l-ylideneaιιιino)-3-methylbenzyl]-5-(trifluoromethyl)-l,3,4- oxadiazole, 2-[4-(4-chloro-3-oxo-3H-isobe--ιzofiu-an-l-ylideneammo)-3-melhylbenzyl]-4-(trifluoromethyl)-2H-
1,2,3-triazole,
2-[4-(4-chloro-3-oxo-3H-isobenzofuran-l-ylideneammo)-3-memylberιzyl]-4-(pentafluoroethyl)- thiazole,
5-[4-(4-chloro-3-oxo-3H-isobenzofuran-l -ylideneamino)-3-methylphenyl]sulfanyl- 1 -methyl-3-(tri- fluoromethyl)-lH-l,2,4-triazole,
3-[4-(4-chloro-3-oxo-3H-isobenzofuran-l-ylideneamino)-3-methylphenyl]-
5-(trifluoromethyl)- 1 ,2,4-oxadiazole,
3-[4-(4-cUoro-3-oxo-3H-isoberιzofuran-l-ylideneamino)-3-methylphenyl]-l-methyl-5-(trifluoro- methyl)-lH-l ,2,4-triazole, 2-[4-(4-iodo-3-oxo-3H-isobenzofuran-l-ylideneamino)-3-methylphenyl]-5-(trifluoromethyl)-l,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 (NUT), 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 (XΗ) with the compounds of the aforementioned formula (HI).
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), Ν,Ν-dimethylaniline, N,N-diethylaniline, pyridine, 4-dimethylaminopyridine (DMAP), l,4-diazabicyclo[2,2,2]octane (DABCO) and l,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 (VIH), there can be mentioned the following: N-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl-methyl]-2-memyl-phenyl}-6-iodo-phthalamic acid, N-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl-methyl]-2-memyl-phenyl}-6-cWoro-ρhthalamic acid, N-{4-[3,5-bis(trifluoromemyl)-(l,2,4)-triazol-l-yl-memyl]-2-me yl-phenyl}-6-iodo-phthalamic acid, N-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-yl]-2-memyl-phenyl}-6-iodo-phthaIamic acid, N-{4-[3,4-bis(pentafluoroethyl)-lH-pyrazol-l-yl-memyl]-phenyl}-6-chloro-ph1halamic acid, N-{4-[3,5-bis entafluoroethyl)-lH-pyrazol-l-yl-methyl]-phenyl}-6-chloro-phthalarnic acid, N-{4-[3,4-bis(heρtafluoropropyl)-lH-pyrazol-l-yl-methyl]-phenyl}-6-chloro-phthalarrric acid, N-{4-[3,5-bis(Tιeptafluoropropyl)-lH-pyrazol-l-yl-memyl]-phenyl}-6-cWoro-phthalamic acid, N-[2-methyl-4-(5-trifluoromethyl-l ,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid, N-[2-memyl-4-(5-pentafluoroethyl-l,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid, N-[2-methyl-4-(5-heptafluoroproρyl-l,3,4-oxadiazol-2-yl)-phenyl]-6-chloro-phthalamic acid, N-[2-methyl-4-(5-trifluoromemyl-l,3,4-oxadiazol-2-yl-methyl)-phenyl]-6-chloro-ρh1halamic acid, N-[2-methyl-4-(4-trifluoromethyl-2H-l,2,3-triazol-2-yl-methyl)-phenyl]-6-chloro-phthalamic acid, N-[2-methyl-4-(4-pentafluoroethyl-1hiazol-2-yl-methyl)-phenyl]-6-chloro-phthalamic acid,
N- {2-methyl-4-[ 1 -methyl-3 -(trifluoromethyl)- 1 H- 1 ,2,4-triazol-5-yl-sufanyl] -phenyl } -6-chloro- phthalamic acid,
N-[2-memyl-4-(5-trifluoromemyl-l,2,4-oxadiazol-3-yl)-phenyl]-6-cWoro-phthalamic acid, N-[2-methyl-4-(l-methyl-5-trifluorome yl-lH-l,2,4-triazol-3-yl)-phenyl]-6-chloro-phthalamic acid, N-[2-methyl-4-(5-trifluoromethyl-l ,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 RIf in the compounds of the formula (If), namely, Ci-ealkylthio- -βalkyl, the compounds of the formula (I), in which the group Rκ corresponds to -β alkylsulfinyl-Cι-6alkyl or Cι-6alkylsulfonyl-Cι-6alkyl, 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-N2-(l-me l-2-methylsulfanyl-e1hyl)-N1-{2-methyl-4-[3,5-bis(1rifluoromethyl)-lH-pyrazol- l-ylmethyl]-phenyl}phthalamide,
N2-(l,l-dimethyl-2-methylsulfanyl-ethyl)-3-iodo-N1-{2-methyl-4-[3,5-bis(trifluoro-methyl)-lH- pyrazol-l-ylmethyl]-phenyl}ρhthalamide,
3-iodo-N2-(l-memyl-2-methylsulfanyl-elhyl)-N1-{2-methyl-4-[3,5-bis(trifluoromethyl)-
(l,2,4)-triazol-l-ylmethyl]-phenyl}phthalarnide, 3-chloro-N2-(l-methyl-2-methylsulfanyl-e l)-N1-{2-me l-4-[3,5-bis(trifluoromethyl)-lH-ρyrazol
-1 -ylmethyl]-phenyl}phthalamide,
3-chloro-N2-(l-me l-2-me lsulf.myl^ zol-l-ylmethyl]-phenyl}phthalamide,
3-cWoro-N2-(l-methyl-2-methylsulf--nyl-ethyl)-N1-{2-methyl-4-[3,5- bis(pentafluoro-ethyl)-lH-pyra- zol- 1 -ylmethyl]-phenyl} phthalamide,
3-chloro-N2-(l-me l-2-methylsulfanyl-ethyl)-N1-{2-methyl-4-[3,4-bis(heptafluoro-propyl)-lH-py- razol-l-ylmethyl]-phenyl}phthalamide,
3-cMoro-N2-(l-me l-2-memylsulfanyl-ethyl)-N1-{2-me l-4-[3,5-bis(heptafluoro-propyl)-lH-py- razol-l-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-dichIoroethane, 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 (IH) to 1 mole of the compounds of the formula (Η) 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, l,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 andbutanol; 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 JJXKEN KAGAKU KOZA (Lecture on experimental chemistry) edited by the Chemical Society of Japan, 4th 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 άlternatus, 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, Galleήa 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.;
Tliysanoptera pests, for example, Tlirips palmi, 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 tritaeniorliynchus, 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; ampro- pylfos; ampropylfos-potassium; andoprim; anilazine; azaconazole; azoxystrobin; benalaxyl; benala- xyl-M; benodanil; benomyl; benthiavalicarb-isopropyl; benzamacril; benzamacril-isobutyl; bilanafos; binapacryl; biphenyl; bitertanol; blasticidin-S; boscalid; bromuconazole; bupirimate; buthiobate; butyl- amine; calcium polysulfide; capsimycin; captafol; captan; carbendazim; carboxin; carpropamid; car- vone; chinomethionat; chlobenthiazone; chlorfenazole; chloroneb; chlorothalonil; chlozolinate; clozyla- con; cyazofamid; cyflufenamid; cymoxanil; cyproconazole; cyprodinil; cyprofuram; Dagger G; deba- carb; dichlofluanid; dichlone; dichlorophen; diclocymet; diclomezine; dicloran; diethofencarb; difeno- conazole; diflumetorim; dimethirimol; dimethomorph; dimoxystrobin; diniconazole; diniconazole-M; dinocap; diphenylamine; dipyrithione; ditalimfos; dithianon; dodine; drazoxolon; edifenphos; epoxicon- azole; ethaboxam; ethirimol; etridiazole; famoxadone; fenamidone; fenapanil; fenarimol; feribucon- azole; fenfuram; fenhexamid; fenitropan; fenoxanil; fenpiclonil; fenpropidin; fenpropimorph; ferbam; fluazinam; flubenzimine; fludioxonil; flumetover; flumorph; fluoromide; fluoxastrobin; fluquincon- azole; flurprimidol; flusilazole; flusulfamide; flutolanil; flutriafol; folpet; fosetyl-Al; fosetyl-sodium; fuberidazole; furalaxyl; furametpyr; furcarbanil; furmecyclox; guazatine; hexachlorobenzene; hexacon- azole; 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; nu- arimol; ofurace; orysastrobin; oxadixyl; oxolinic acid; oxpoconazole; oxycarboxin; oxyfenthiin; paclo- butrazol; pefurazoate; penconazole; pencycuron; phosdiphen; phthalide; picoxystrobin; piperalin; poly- oxins; polyoxorim; probenazole; prochloraz; procymidone; propamocarb; propanostne-sodium; propi- conazole; propineb; proquinazid; prothioconazole; pyraclostrobin; pyrazophos; pyrifenox; pyrimethanil; pyroquilon; pyroxyfur; pyrrolnitrine; quinconazole; quinoxyfen; quintozene; simeconazole; spirox- amine; sulfur; tebuconazole; tecloftalam; tecnazene; tetcyclacis; tetraconazole; thiabendazole; thicyo- fen; thifluzamide; thiophanate-methyl; thiram; tioxymid; tolclofos-methyl; tolylfluanid; triadimefon; triadimenol; triazbutil; triazoxide; tricyclamide; tricyclazole; tridemoiph; trifloxystrobin; triflumizole; triforine; triticonazole; uniconazole; validamycin A; vinclozolin; zineb; ziram; zoxamide; (2S)-N-[2-[4- [[3-(4-cUorophenyl)-2-propynyl]oxy]-3-memoxyphenyl]ethyl]-3-me yl-2-[(me ylsιιlfonyl)amino]- butanamide; l-(l-naphthalenyl)-lH-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-l,l,3-trimethyl-lH-in- den^l-yl)-3-pyridinecarboxa ide; 3,4,5-trichloro-2,6-pyridinedicarbor-itrile; actinovate; cis-l-(4-chloro- ρhenyl)-2-(lH-l,2,4-triazol-l-yl)-cycloheptanol; methyl l-(2,3-dihydro-2,2-dimethyl-lH-inden-l-yl)- lH-imidazole-5-carboxylate; mono potassium carbonate; N-(6-methoxy-3-pyridinyl)-cyclopropane- carboxamide; N-butyl-8-(l,l-dimemylethyl)-l-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, chloethocarb, 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, di- crotophos, dimethoate, dimethylvinphos, dioxabenzofos, disulfoton, epn, ethion, ethoprophos, etrimfos, famphur, fenamiphos, fenitrothion, fensulfothion, fenthion, flupyrazofos, fonofos, formothion, fos- methilan, fosthiazate, heptenophos, iodofenphos, iprobenfos, isazofos, isofenphos, isopropyl o-salicyl- ate, isoxathion, malathion, mecarbam, methacrifos, methamidophos, methidathion, mevinphos, mono- crotophos, naled, omefhoate, oxydemeton-methyl, parathion (-methyl -ethyl), phenfhoate, 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 Mockers
2.1 Pyrethroids (e.g. acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, bioallethrin, bioallethrin-s-cyclopentyl-isomer, bioethanomethiin, biopermethrin, bioresmethrin, cWovaporthrin, cis-cypermethrin, cis-resmethrin, cis-permethrin, clocythrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, DDT, deltamethrin, empenthrin (lR-isomer), esfenvalerate, etofenprox, fenfluthrin, fenpropathrin, fenpyrithrin, fenvalerate, flubrocythrinate, flucythrinate, flufenprox, flumethrin, fluvalinate, fubfenprox, gamma-cyhalothrin, imiprothrin, kadethrin, lambda-cyhalothrin, metofluthrin, permethrin (cis-, trans-), phenothrin (lR-trans isomer), prallethrin, profluthrin, protrifenbute, pyresmethrin, resmethrin, RU 15525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin, tetramethrin (lR-isomer), tralomethrin, transfluthrin, ZXI 8901, pyrethrins (pyrethrum))
2.2 Oxadiazine (e.g. indoxacarb)
3. Acetylcholine receptor agonistsf-antagonists
3.1 Chloronicotinyls/neonicotinoids (e.g. acetamiprid, clothianidin, dinotefiiran, imidacloprid, niten- pyram, 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 ofchitin biosynthesis
9.1 Benzoylureas (e.g. bistrifluron, chlofluazuron, diflubenzuron, fluazuron, flucycloxuron, flu- fenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, triflumuron) 9.2 buprofezin
9.3 cyromazine
10. Inhibitors of oxidative phosphorylation, ATP-dismptors
10.1 diafenthiuron
10.2 Organotins (e.g. azocyclotin, cyhexatin, fenbutatin-oxide) 11. Decoupler of oxidative phoshorylation by diruption 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 Teframic acid insecticides [e.g. 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-l-azaspiro[4.5]dec-3- en-4-yl ethyl carbonate (alias: carbonic acid, 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-l-azaspiro[4.5]- dec-3-en-4-yl ethyl ester, CAS-Reg.-No.: 382608-10-8) and carbonic acid, cis-3-(2,5-dimethylphe- nyl)-8-methoxy-2-oxo-l-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. N2-[l,l-dimemyl-2-(me lsulfonyl)e l]-3-iodo-N1-[2-me l-4-[l,2,2,2-tettafluoro-l-(trifluoro- memyl)ethyl]phenyl]-l,2-benzenedicarboxamide (CAS-Reg.-No.: 272451-65-7, flubendiamide))
21. Nereistoxin analogues
(e.g. thiocyclam hydrogen oxalate, thiosultap-sodium)
22. Biologica, hormones orpheromones (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 Mockers (e.g. cryolite, flomcamid, pymetrozine) 23.3 Mite growth inhibitors (e.g. clofentezine, etoxazole, hexythiazox)
23.4 amidoflumet, benclothiaz, benzoximate, bifenazate, bromopropylate, buprofezin, chinomethio- nat, 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- ρyridinyl)-8-(2,2,2-trifluoroe l)-8-azabicyclo[3.2.1]octøn-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 defence 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 defence 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), CryllA, CrylllA, CryIDB2, Cry9c, Cry2Ab, Cry3Bb and CrylF and also combinations thereof) (hereinbelow referred to as "Bt plants"). Traits that are also particularly emphasized are the increased defence 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), DVH® (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
Figure imgf000039_0001
3-(l,l-Dimemyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofiιran-l-one (0.53 g) and l-(3-me- thyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-lH-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
Figure imgf000039_0002
methylpyrazol-l-ylmethyl)-2-methylphenyl]-N2-(l,l-dimethyl-2-methylsulfanylethyl)-3-iodophthal- amide (0.91 g). mp. 83-87°C.
Synthesis Example 2
Figure imgf000039_0003
Nl-{4-[3,5-Bis(1rifluoromethyl)-lH-ρyrazol-l-ylme l]-2-me lphenyl}-N2-(l,l-dimethyl-2-me%l- sulfanylethyl)-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 N1-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol- l-ylmethyl]-2-methylphenyl}-N2- (2-methanesulfinyl-l,l-dimethylethyl)-3-iodophthalamide (0.30 g).
'H-NMR (CDC13, 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
Figure imgf000040_0001
Nl-{4-[3,5-Bis(trifluoromethyl)-lH-pyrazol-l-ylme1hyl]-2-methylphenyl}-N2- (l,l-dimethyl-2-methyl- sulfanylethyl)-3-iodophthalamide (0.30 g) was dissolved in dichloromethane, to which m-chloroperben- zoic 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 N1-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-ylmethyl]-2- me lphenyl}-3-iodo-N2-(2-memanesulfonyl-l,l-dimethylethyl)phthalamide (0.25 g). mp. 104-107°C.
Synthesis Example 4
Figure imgf000040_0002
A dioxane solution (15 ml) of 2-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l- ylmethyl]-2-methyl- phenyl}-4-fluoroisoindole-l,3-dione (0.94 g), (S)-l-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 N1-{4-[3,5-bis(trifluoromethyl)-lH-pyrazol-l-ylmethyl]-2-methylphenyl}-3-fluoro-N2-[l-(S)-l- methyl-2-methylsulfanyl-ethyl]-phthalamide (0.19 g) (compound No. 549). mp. 66-68°C. Synthesis Example 5
Figure imgf000041_0001
3-Iodo-N-(l,l-dimethyl-2-methylsulfanyl-ethyl)-phthalamic acid (0.39 g) and N-(3-dimethylamino- propy^-N1 -ethylcarbonyl diimidazole hydrochloride (0.19 g) were stirred in dichloromethane (10 ml) at room temperature for 30 minutes. Then, 2-methyl-4-[l-(3-trifluoromethyl-lH-pyrazol-l-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 N2-(l,l-dimethyl-2-methylsulf--nyl-ethyl)-3-iodo-N1-{2-me l-4-[l-(3-trifluoromethyl-lH-pyrazol-l -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
Figure imgf000041_0002
Q1 Q2 Q3 Q4 Q5
Figure imgf000042_0001
Q6 Q7 Q8 Q9 Q10
Figure imgf000042_0002
Q11 Q12 Q13 Q14 Q15 DDD! DDDDDDDDDDDDD
Figure imgf000042_0003
Figure imgf000043_0001
Figure imgf000044_0001
Figure imgf000045_0001
Figure imgf000046_0001
Figure imgf000047_0001
Figure imgf000048_0001
Figure imgf000049_0001
Figure imgf000050_0001
Figure imgf000051_0001
Figure imgf000052_0001
Figure imgf000053_0001
Figure imgf000054_0001
Figure imgf000055_0001
Figure imgf000056_0001
Figure imgf000057_0001
Figure imgf000058_0001
Figure imgf000059_0001
Figure imgf000060_0001
Figure imgf000061_0001
Figure imgf000062_0001
Figure imgf000063_0001
Figure imgf000064_0001
Figure imgf000065_0001
Figure imgf000066_0001
Figure imgf000067_0001
Figure imgf000068_0001
Table 2 No. I 1 H-NMR (CDCI3, ppm):1.4 (6H, s), 2.0 (3H, s), 2.3 (3H, s), 2.9 (2H, s), 5.4 (2H, s), 6.2 (1 H, s), 6.9 (1 H, s), 7.3-8.7 (8H, m) 3 1 H-NMR (CDCI3, ppm):1.5 (6H, s), 2.2 (3H, s), 2.6 (3H, s), 3.7 (2H, s), 5.4 (2H, s), 6.4 (1 H, s), 6.9 (1 H, s), 7.3-8.2 (8H, m) 8 1 H-NMR (CDCI3, ppm):1.4 (6H, s), 2.0 (3H, s), 2.3 (3H, s), 2.9 (2H, s), 5.4 (2H, s), 6.1 (1 H, s), 6.9 (1 H, s), 7.3-8.4 (7H, m) I I 1 H-NMR (CDCI3, ppm):1.2 (3H, d), 1.9 (3H, s), 2.3 (3H, s), 2.7 (2H, dd), 4.2 (1 H, m), 5.4 (2H, s), 6.4 (1 H, d), 6.9 (1H, s), 7.3-8.4 (7H, m) 15 1 H-NMR (CDCI3, 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 (1 H, d), 6.9-8.4 (8H, m) 47 1 H-NMR (CDCI3, 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) 52 1 H-NMR (CDCI3, ppm):1.4 (3H, d), 2.2 (3H, s), 2.7 (3H, s), 3.2 (2H, m), 4.4 (1 H, m), 5.4 (2H, s), 6.9-8.2 (9H, m) No.
81 1 H-NMR (CDCI3, ppm):1.1 (6H, d), 2.2 (3H, s), 4.2 (1H, m), 5.3 (2H, s), 5.9 (1 H, d), 6.9-8.2 (8H, m)
83 1 H-NMR (CDCI3, 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) 85 1 H-NMR (CDCI3, ppm):1.2 (3H, d), 1.8 (3H, s), 2.2 (3H, s), 2.6 (2H, dd), 4.2 (1 H, m), 5.3 (2H, s), 6.5 (1H, d), 6.9 (1H, s), 7.3-8.4 (7H, m) 89 1 H-NMR (CDCI3, ppm):1.4 (3H, d), 2.2 (3H, s), 2.7 (3H, s), 3.2 (2H, m), 4.5 (1 H, m), 5.3 (2H, s), 6.6 (1H, d), 6.9-7.9 (8H, m) 94 1 H-NMR (CDCI3, 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 (1 H, s), 6.90 (1 H, s), 7.0-8.2 (7H, m)
96 1 H-NMR (CDCI3, ppm):1.63 (6H, s), 2.27 (3H, s), 2.50 (3H, s), 3.47 (2H, s), 5.30 (2H, s), 6.23 (1 H, s), 6.57 (1H, s), 7.0-8.1 (8H, m)
97 1 H-NMR (CDCI3, ppm):1.27 (3H, d), 1.93 (3H, s), 2.30 (3H, s), 2.63 (2H, m), 4.33 (1 H, m), 5.37 (2H, s), 6.07 (1H, m), 6.60 (1H, s), 6.9-8.2 (8H, m) 99 1 H-NMR (CDCI3, ppm):1.50 (3H, d), 2.27 (3H, s), 2.70 (3H, s), 3.0-3.5 (2H, m), 4.60 (1 H, m), 5.37 (2H, s), 6.5-8.0 (1 OH, m) 103 1 H-NMR (CDCI3, 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 (1 H, t), 7.1-8.3 (8H, m) 107 1 H-NMR (CDCI3, 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) 116 1 H-NMR (CDCI3, 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) 149 1 H-NMR (CDCI3, 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 (1 H, d), 8.49 (1H, s) 153 1 H-NMR (CDCI3, ppm): 1.22 (3H, d), 2.05 (3H, s), 2.30 (3H, s), 2.61-2.53 (2H, m), 4.40-4.29 (1 H, 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) 180 1 H-NMR (CDCI3, 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) 242 1 H-NMR (CDCI3, ppm):1.4 (3H, d), 2.2 (3H, s), 2.8 (3H, s), 3.2 (2H, m), 4.6 (1 H, m), 5.5 (2H, s), 6.2-8.2 (9H, m) 251 1 H-NMR (CDCI3, 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) 271 1 H-NMR (CDCI3, ppm):1.47 (6H, s), 2.00 (3H, s), 2.30 (3H, s), 2.83 (2H, s), 3.30 (1 H, m), 4.2-4.6 (4H, m), 6.07 (1H, s), 7.1-8.2 (7H, m) 277 1 H-NMR (CDCI3, 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) 417 1 H-NMR (CDCI3, 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) 422 1 H-NMR (CDCI3, ppm):1.47 (6H, s), 2.03 (3H, s), 2.40 (3H, s), 2.87 (2H, s), 6.03 (1 H, s), 6.80 (1 H, m), 7.1-8.6 (8H, m) 434 1 H-NMR (CDC13, ppm):1.40 (6H, s), 2.03 (3H, s), 2.40 (3H, s), 2.87 (2H, s), 6.07 (1 H, s), 6.77 (1 H, m), 7.2-8.5 (8H, m)
521 1 H-NMR (CDCI3, 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 (1 H, bs), 6.90-7.20 (3H, m), 7.57 (1H, bs), 7.70 (1H, d), 7.80-8.23 (3H, m)
522 1 H-NMR (CDCI3, 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 (1 OH, m)
523 1 H-NMR (CDCI3, 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)
529 1 H-NMR (CDCI3, ppm):1.42 (6H, s), 1.98 (3H, s), 2.30 (3H, s), 2.71 (2H, s), 5.30 (2H, s), 6.03 (1 H, 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)
530 1 H-NMR (CDCI3, ppm):1.63 (6H, s), 2.30 (3H, s),2. 57 (3H, s), 3.47 (2H, s), 5.30 (2H, s), 6.40 (1 H, bs), 6.57 (1H, d), 7.03-8.17 (8H, m) 532 1 H-NMR (CDCI3, ppm):1.30 (4H, dd), 1.97 (3H, s), 2.28 (3H, s), 2.73-2.42 (2H, m), 4.37-4.28 (1 H, 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 (1 H, t), 8.02 (1 H, d), 8.49 (1H, d) 534 1 H-NMR (CDCI3, 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 (1 H, d), 6.54 (1 H, d), 7.06 (1 H, bs), 7.11 (1 H, d), 7.22 (1 H, t), 7.40 (1 H, d), 7.78 (1H, d), 7.97 (1H, d), 8.17 (1H, d), 8.30 (1H, bs) 536 1 H-NMR (CDCI3, 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) No.
537 1 H-NMR (CDC13, 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)
538 1 H-NMR (CDCI3, 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) 550 1 H-NMR (CDCI3, ppm):1.48 (6H, d), 2.21 (3H, s), 2.48 (3H, s), 4.13 (1H, m), 5.42 (2H, s), 6.18(1 H, d), 6.91 (1H, s), 7.1-7,6 (6H, m), 8.08 (1 H, d) 552 1 H-NMR (CDCI3, 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)
553 1 H-NMR . (CDCI3, 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)
554 1 H-NMR (CDCI3, 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)
569 1 H-NMR (CDCI3, 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 (1 H, q), 4.38 (1 H, m), 2.79 (2H, m), 2.29 (3H, s), 2.20 (3H, s), 2.00 (3H, d), 1.43-1.18 (3H, d)
574 1 H-NMR (CDCI3, 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)
594 1 H-NMR (CDCI3, 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)
595 1 H-NMR (CDCI3, 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 (1 H, d), 7.93 (1H, dd), 8.05 (1H, d), 8.36 (1H, s)
596 1 H-NMR (CDCI3, 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 (1 H, m), 7.35-7.32 (1H, m), 7.42-7.39 (1 H, m), 7.80 (1 H, t), 7.98 (1 H, d), 8.18 (1 H, t), 8.32 (1 H, d)
626 1 H-NMR (CDCI3, 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 (1 H, d), 8.07 (1 H, d), 8.38 (1 H, bs)
632 1 H-NMR (CDCI3, 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)
633 1 H-NMR (CDCI3, 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 (1 H, t), 7.48 (1 H, dd), 7.61-7.53 (1H, m), 7.79 (1H, dt), 8.15 (1H, d),8.43 (1H, d)
634 1 H-NMR (CDCI3, 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)
635 1 H-NMR (CDCI3. 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)
636 1 H-NMR (CDCI3, 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 (1 H, s), 7.74 (1H, d), 7.94 (1H, d),8.11 (1H, d)
640 1 H-NMR (CDCI3, 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)
651 1 H-NMR (CDCI3, 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 (1 H, d), 8.12 (1H, d), 8.50 (1 H, s)
654 1 H-NMR (CDCI3, 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)
658 1 H-NMR (CDCI3, 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) No.
660 1 H-NMR (CDCI3, ppm):1.25 (4H, dd), 1.90 (3H, s), 2.31 (3H, s), 2.63-2.55 (2H, m), 4.37-4.28 (1 H, m), 5.34 (2H, s), 6.12 (1H, d), 7.22-7.15 (2H, m), 7.63 (1H, d), 7.83 (1 H, t), 7.98 (1H, dt), 8.25 (1H, t),8.34 (1H, s) 675 1 H-NMR (CDCI3, 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 (1 H, d), 7.73 (1H, d), 7.84 (1H, s), 8.07 (1H, d), 8.38 (1H, s) 681 1 H-NMR (CDCI3, ppm): 1.25 (3H, d), 1.95 (3H, s), 2.32 (3H, s), 2.62-2.54 (2H, m), 4.36-4.32 (1 H, 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) 714 1 H-NMR (CDCI3, 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)
726 1 H-NMR (CDCI3, ppm): 1.45-1.37 (3H, m), 2.32-2.30 (6H, m), 2.87-2.83 (2H, m), 4.61-4.46 (1 H, 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)
727 1 H-NMR (CDCI3, ppm): 1.44 (3H, d), 2.30 (3H, s), 2.75 (3H, s), 3.24-3.21 (2H, m), 4.62-4.53 (1 H, 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 (1 H, m), 7.60-7.57 (1H, m), 7.77 (1H, s), 7.91-7.87 (1H, m), 8.17-8.14 (1H, m)
729 1 H-NMR (CDCI3, ppm): 1.45 (3H, d), 2.29 (3H, s), 2.75 (3H, s), 3.34-3.12 (2H, m), 4.59-4.54 (1 H, 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)
730 1 H-NMR (CDCI3, 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) 741 1 H-NMR (CDCI3, 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) 778 1 H-NMR (CDCI3, ppm): 1.31 (3H, d), 1.95 (3H, s), 2.33 (3H, t), 2.61-2.56 (2H, m), 4.40-4.29 (1 H, 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 (1 H, m), 7.64 (1H, s), 7.72 (1 H, d), 8.12 (1H, d), 8.50 (1H, s) 799 1 H-NMR (CDCI3, ppm): 1.23 (3H, d), 1.93 (3H, s), 2.32 (3H, s), 2.56 (2H, m), 4.22 (1 H, 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) 1 H-NMR (CDCI3, 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 (1 H, d), 8.41 (1H, bs) 1 H-NMR (CDCI3, ppm): 1.40 (6H, s), 1.93 (3H, s), 2.77 (2H, s), 5.40 (2H, s), 5.93 (1 H, bs), 6.87-7.23 (4H, m), 7.63-7.95 (2H, m), 8.35-8.65 (2H, m)
Synthesis Example 6 (Starting material)
Figure imgf000071_0001
3-Methyl-4-nitrobenzyl chloride (1.81 g), 3,5-bis(trifluoromethyl)-lH-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 l-(3-methyl-4-mtrober-zyl)-3,5-bis-(trifluoromethyl)-lH-pyrazole (3.3 g). Η-NMR (CDCI3, ppm): 2.59 (3H, s), 5.50 (2H, s), 6.90 (1H, s), 7.1-7.2 (2H, m), 8.00 (1H, d).
Figure imgf000072_0001
To a mixture of l-(3-methyi-4-nitrobenzyl)-3,5-bis(trifluoromethyl)-lH-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 l-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-lH-pyrazole (1.19 g). Η-NMR (CDC13, 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)
Figure imgf000072_0002
l-(3-Methyl-4-nitrobenzyl)-3,5-bis (trifluoromethyl)-lH-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, IN 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, l-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoro- methyl)-lH-pyrazole (13.0 g), which was the same as that obtained in Synthesis Example 7, was obtained.
Synthesis Example 9 (Starting material)
Figure imgf000072_0003
3-Fluorophthalic anhydride (4.98 g) and l-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-lH- 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)-lH-pyrazol-l-yl- methyl]-2- methylρhenyl}-4-fluoroisoindol-l,3-dione (10.80 g).mρ. 158-159°C.
Synthesis Example 10 (Starting material)
Figure imgf000073_0001
3-Methyl-4-nitrobenzyl chloride (0.56 g), 5-(difluoromethyl)-l,2-dihydro-2-methyl-3H-l,2,4-(tri- azol)-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-[l,2,4]triazol-3-one (0.45 g). Η-NMR (CDCI3, 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)
Figure imgf000073_0002
3-Methyl-4-nitrobenzyl chloride (0.43 g), 3-heptafluoropropylsulfanyl-5-trifluoromethyl-lH-(l,2,4)-tri- azole (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-hepta- fluoropropylsulfanyl-l-(3-memyl-4-nitrobeιιzyl)-5-trifluoromemyl-lH-(l,2,4)-triazole (0.30 g). 'H-NMR (CDCI3, 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)
Figure imgf000074_0001
• To a mixture of 3-heptafluoropropyls fanyl-l-(3-me l-4-m^ophenyl)-5-trifluoromethyl-lH-(l,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-h tafluoropropylsulfanyl-5-trifluoromemyl-[l,2,4]1riazol-l-ylmethyl)-2-methyl-ρhenyl- amine (0.28 g) 'H-NMR (CDC13, 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)
Figure imgf000074_0002
An acetonitrile solution (30 ml) of 3-trifluoromethyl-lH-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-lH-pyrazole (9.3 g). 'H-NMR (CDCI3, ppm): 7.77 (1H, s).
Synthesis Example 14 (Starting material)
Figure imgf000074_0003
3-Methyl-4-nitrobenzyl chloride (0.77 g), 4-iodo-3-trifluoromethyl-lH-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-l- (3-methyl-4-nitrobenzyl)-3-trifluoromethyl-lH-pyrazole (1.0 g). 'H-NMR (CDC13, 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)
Figure imgf000075_0001
4-Iodo-l-(3-methyl-4-nitrober-zyl)-3-trifluoromethyl-lH-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 l-(3-methyl-4-nitro- benzyl)-4-pentafluoroethyl-3-trifluoromethyl-lH-pyrazole (1.39 g) 'H-NMR (CDCI3, 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)
Figure imgf000075_0002
3-Methyl-4-nitrobenzyl chloride (8.57 g), 4-iodo-3-pentafluoroethyl-lH-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-l-(3-methyl-4---itrobenzyl)-3-pentafluoro- ethyl-lH-pyrazole (4.60 g). 'H-NMR (CDCI3, 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)
Figure imgf000075_0003
4-Iodo- 1 -(3 -methyl-4-nitrobenzyl)-3 -pentafluoroethyl-1 H-pyrazole (1.84g), (trifluoromethyl)trime- thylsilane (1.14g), copper(I) iodide (1.52g), potassium fluoride (0.28g) 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 l-(3-me- thyl-4-mtro-benzyl)-3-pentafluoroethyl-4-trifluoromethyl-lH-pyrazole (0.32g).
'H-NMR (CDC13, 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)
Figure imgf000076_0001
4-Iodo-l-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-lH-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 l-(3-methyl-4-nitro- benzyl)-4-pentafluoropropyl-3- trifluoromethyl-lH-pyrazole (0.80 g). 'H-NMR (CDCI3, 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)
Figure imgf000076_0002
4-Iodo-l-(3-methyl-4-nitrobenzyl)-3-trifluoromethyl-lH-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 l-(3-methyl-4-nitro- benzyl)-4-nonafluorobutyl-3- trifluoromethyl-lH-pyrazole (1.50 g). Η-NMR (CDCI3, 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)
Figure imgf000077_0001
An acetonitrile solution (20 ml) of 3-trifluoromethyl-lH-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-lH-pyrazole (1.6 g). 'H-NMR (CDC13, ppm): 7.73 (IH, s), 12.86 (IH, brs). Synthesis Example 21 (Starting material)
Figure imgf000077_0002
3-Methyl-4-nitrobenzyl chloride (0.77 g), 4-bromo-3-trifluoromethyl-lH-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 l-(3-methyl-4-nitrobenzyl)-4-bromo-3-trifluoromethyl-lH-pyrazole (0.9 g). 'H-NMR (CDCI3, ppm): 2.58 (3H, s), 5.35 (2H, s), 7.24-7.21 (2H, m), 7.49 (IH, s), 7.98 (IH, d).
Synthesis Example 22 (Starting material)
Figure imgf000077_0003
An acetonitrile solution (20 ml) of 3-trifluoromethyl-lH-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- IH- pyrazole (0.9 g). 'H-NMR (CDCI3, ppm): 7.80 (IH, s). Synthesis Example 23 (Starting material)
Figure imgf000078_0001
3-Methyl-4-nitrobenzyl chloride (0.82 g), 4-chloro-3-trifluoromethyl-lH- 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 l-(3-methyl-4-nitrober-zyl)-4-chloro-3-trifluoromethyl- lH-pyrazole (0.98 g). 'H-NMR (CDC13, ppm): 2.62 (3H, s), 5.33 (2H, s), 7.21-7.19 (2H, m), 7.46 (IH, s), 7.98 (IH, d).
Synthesis Example 24 (Starting material)
Figure imgf000078_0002
2-(Trifluroacetyl)-lH-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 l-(3-methyl-4-nitrobeiizyl)-2- (trifluoroacetyl)-lH-pyrrole (1.53 g). 'H-NMR (CDCI3, ppm): 2.55 (3H, s), 5.59 (2H, s), 6.44-6.41 (IH, m), 6.99 (IH, d), 7.04 (IH, s), 7.22-7.19 (IH, m), 7.35-7.32 (IH, m), 7.93 (IH, d).
Synthesis Example 25 (Starting material)
Figure imgf000078_0003
An acetonitrile solution (20 ml) of 2-(trifluoroacetyl)-lH-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)-lH-pyrrole (0.6 g). 'H-NMR (CDCI3, ppm): 7.28-7.35 (2H, m), 9.52 (IH, brs). Synthesis Example 26 (Starting material)
Figure imgf000079_0001
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 solu- tion 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-l- (3-methyl-4-nitrobenzyl)-2-trifluoroacetyl- lH-pyrrole (0.45 g). 'H-NMR (CDC13, ppm): 2.60 (3H, s), 5.56 (2H, s), 7.05-7.12 (2H, m), 7.21 (IH, d), 7.39 (IH, s), 7.94 (IH, d).
Synthesis Example 27 (Starting material)
Figure imgf000079_0002
4-Iodo-l-(3-methyl-4-nitroberιzyl)-2-trifluoroacetyl-lH-pyrrole (1.75 g), copper powder (5.08 g), iodo- pentafluoroethane (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-lH-pyrrole (1.35 g).
'H-NMR (CDCI3, ppm): 2.59 (3H, s), 5.62 (2H, s), 7.00-7.10 (2H, m), 7.43-7.50 (2H, m), 7.96 (IH, d).
Some specific examples of other processes to synthesize the compounds of the aforementioned formula (IX) are shown below.
Synthesis Example 28 (Starting material)
Figure imgf000079_0003
To a toluene suspension of ethyl 4,4,4-trifluoroacetoacetate (5.0 g), sodium hydride (1,1 g) was slowly added and the mixture was stirred for 1 hour. After adding 4-chloromethyl-2-me- thyl-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 IN 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). nD 20 1.4970
Synthesis Example 29 (Starting material)
Figure imgf000080_0001
Ethyl 4,4,4-trifluoro-2- (3-methyl-4-nitro-benzyl)-3-oxo-butyrate (2.0 g), hydrazine mono-hydrate (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 IN 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-tri- fluoromethyl-2,4-dihydro-pyrazol-3-one (1.0 g).
'H-NMR (DMSO-dfo 90MHz): 82.2 (3H, s), 3.8 (2H, s), 7.0 (IH, d, J=5.5Hz), 7.2 (IH, s), 7.8 (IH, d, J=5.5Hz), 11.2 (lH, brs).
Synthesis Example 30 (Starting material)
Figure imgf000080_0002
To a DMF suspension of 4-(3-me yl-4-mtro-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-l-difluoromethyl-4-(3- methyl-4-nitro-benzyl)-3-trifluoromethyl-lH-pyrazole (EX-1) (0.5 g) and 3-difluoromethoxy-l-difluoro- methyl-4- (3-methyl-4-nitro-benzyl)-5-trifluoromethyl-lH-pyrazole (K-2) (0.4 g) respectively. CK-1): nD 20 1.4780, (K-2): nD 20 1.4855.
Synthesis Example 31 (Starting material)
Figure imgf000081_0001
(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 l-(3-methyl-4-nitro- pheιiyl)-3,5- bis(trifluoromethyl)-lH-pyrazole (5.6 g). nD 20 1.4890.
Synthesis Example 32 (Starting material)
Figure imgf000081_0002
(3-Methyl-4-nitro-phenyl)-hydrazine (2.0 g) . and l,l,l,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 l-(3-methyl-4-nitro-phenyl)-3- pentafluoroethyl-5-trifluoromethyl-lH-pyrazole (K-3) (3.0 g) and
2-(3-memyl-4-nitro-phenyl)-5-pentafluoroethyl-3-trifluoromemyl-3,4-dihydro-2H-pyrazol-3-ol (K-4)
(0.5 g), respectively. (K-3): nD 20 1.4690,
(K-4): 'H-NMR (CDC13, 90MHz): 52.6 (3H, s), 3.3 (IH, br d, J=16Hz), 3.7 (IH, br d, J=16Hz), 4.1
(IH, s), 7.2 (2H, m), 7.8 (IH, d, J=7.8Hz).
Synthesis Example 33 (Starting material)
Figure imgf000081_0003
To a THF suspension of l-(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 IN 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-l- (3-methyl-4-nitro-phenyl)-butane-l,3- dione (2.5 g). 'H-NMR (CDCI3, 90MHz): 52.6 (3H, s), 6.5 (IH, s), 7.7-8.1 (3H, m).
Synthesis Example 34 (Starting material)
Figure imgf000082_0001
A toluene solution of 4,4,4-trifluoro-l-(3-methyl-4-nitro-phenyl)-butane-l,3-dione (1.8 g), 2,2,2-tri- fluoroethylhydrazine (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-memyl-4-nitro-phenyl)-l-(2,2,2-1rifluoro-ethyl)-5-trifluoro-methyl-lH- pyrazole (K-5) (1.1 g) and 5-(3-methyl-4-nitro-phenyl)-l- (2,2,2-trifluoro-ethyl)-3-trifluoromethyl-lH- pyrazole (K-6) (0.5 g), respectively. (K-5) mp; 98-104°C, (K-6) mp; 50-53°C.
Synthesis Example 35 (Starting material)
Figure imgf000082_0002
To a dichloromethane solution of 2,2-dimethyl-l,3-dioxane-4,6-dione (10 g) and dimethylamino- pyridine (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 IN 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-me- thyl-4-nitro-phenyl)-3-oxo- propionate (12.4 g). mp; 207-211°C. Synthesis Example 36 (Starting material)
Figure imgf000083_0001
To an ethanol solution of ethyl 3-(3-methyl-4-nitro-phenyl)-3-oxo-ρropionate (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)
Figure imgf000083_0002
To a DMF suspension of 5-(3-methyl-4-nitro-phenyl)-2,4-dihydro-lH-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-l-difluoromethyl-3-(3-methyl-4- nitro-phenyl)-lH-pyrazole (K-7) (0.7 g) and 3-difluoromethoxy-l-difluoromethyl-5-(3-methyl-4- nitro-phenyl)-lH- pyrazole (K-8) (0.5 g), respectively. (K-7) mp; 80-82°C, (K-8) mp; 99-100°C.
Synthesis Example 38 (Starting material)
Figure imgf000083_0003
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. 'H-NMR (CDClj, ppm): 2.60 (3H, s), 2.65-3.35 (3H, m), 3.95 (2H, s), 7.20-7.40 (2H, m), 7.98 (IH, d). Synthesis Example 39 (Starting material)
Figure imgf000084_0001
(3-Methyl-4-nitrobenzyl)-hydrazine (1.81 g) and 5-ethoxy-l,l,l,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 l-(3-methyl-4-nitrobenzyl)-5-pentafluoro- ethyl-lH-pyrazole (0.96 g) as the first elution portion and l-(3-methyl-4-nitrobenzyl)-3-pentafluoro- ethyl-lH-pyrazole (0.50 g) as the second elution portion.
(K-9): 'H-NMR (CDC13, ppm): 2.61 (3H, s), 5.49 (2H, s), 6.70 (IH, bs), 7.05-7.15 (2H, m), 7.66 (IH, bs), 7.94 (IH, d).
(K-10): 'H-NMR (CDC13, ppm): 2.64 (3H, s), 5.40 (2H, s), 6.63 (IH, d), 7.07-7.20 (2H, m), 7.52 (IH, d), 7.95 (lH, d).
Synthesis Example 40 (Starting material)
Figure imgf000084_0002
A mixture of 5-fluoro-2-nitrotoluene (2.33 g), 4-iodo-lH-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-l-(3-methyl-4-nitro- phenyl)-lH-pyrazole (4.60 g) was obtained. 'H-NMR (CDCI3, ppm): 2.70 (3H, s), 7.50-7.70 (3H, m), 7.95-8.15 (2H, m).
Synthesis Example 41 (Starting material)
Figure imgf000084_0003
4-Iodo-l-(3-methyl-4-nitrophenyl)-lH-pyrazole (1.98 g), copper powder (1.14 g), iodopentafluoro- ethane (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 l-(3-methyl-4-nitrophenyl)-4-pentafluoroethyl- lH-pyrazole (0.72 g). 'H-NMR (CDC13, ppm): 2.70 (3H, s), 7.60-7.73 (2H, m), 7.93 (IH, s), 8.13 (IH, d), 8.23 (IH, s).
Synthesis Example 42 (Starting material)
Figure imgf000085_0001
To a suspension of methanol (300 ml) of 3-methyl-4-nitroacetophenone (26.88 g), sodium boro- hydride (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 l-(3-methyl-4-nitrophenyl)-ethanol (23.33 g) was obtained. 'H-NMR (CDCI3, ppm): 1.51 (3H, d), 1.98 (IH, d), 2.62 (3H, s), 4.90-5.01 (IH, m), 7.28-7.35 (2H, m), 7.98 (IH, d).
Synthesis Example 43 (Starting material)
Figure imgf000085_0002
Into a THF solution (35 ml) of l-(3-methyl-4-nitrophenyl)-ethanol (5.44 g) and triethylamine (3.95 g), a THF solution (10 ml) of mefhanesulfonyl 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 l-(3-methyl-4-nitrophenyl)-ethyl methanesulfonate (5.80 g) was obtained.
'H-NMR (CDCI3, ppm): 1.74 (3H, d), 2.65 (3H, s), 2.95 (3H, s), 5.76 (IH, q), 7.35-7.45 (2H, m), 8.01 (IH, d). Synthesis Example 44 (Starting material)
Figure imgf000086_0001
l-(3-Methyl-4-nitrophenyl)-ethyl methanesulfonate (2.59 g), 3-trifluoromethyl-lH-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 l-[l-(3-methyl-4-nitrophenyl)-ethyl]-3-tri- fluoromethyl- lH-pyrazole (1.60 g). 'H-NMR (CDC13, ppm): 1.95 (3H, d), 2.59 (3H, s), 5.59 (IH, q), 6.57 (IH, bs), 7.13-7.20 (2H, m), 7.47 (lH, bs), 8.00 (lH, d).
Synthesis Example 45 (Starting material)
Figure imgf000086_0002
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-lH- (l,2,4)-triazole (7.9 g).
Synthesis Example 46 (Starting material)
Figure imgf000086_0003
l-(3-Methyl-4-nitrophenyl)-ethyl methanesulfonate (2.5 g), 3-pentafluoroethyl-5-trifluoromethyl-lH- (l,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 (K-l l) l-([l-(3-methyl-4-nitro-phenyl)-ethyl]-5- pentafluoroethyl-3-trifluoromethyl- lH-(l,2,4)-triazole (0.95 g) as the first elution portion and (K-12) l-([l-(3-methyl~4- nitro-phenyl)-ethyl]-3-pentafluoroethyl-5-trifluoromethyl-lH-(l,2,4)-tri- azole (1.35 g) as the second elution portion. (K-ll)
'H-NMR (CDCl3)δ: 8.03-7.97 (IH, m), 7.37 (2H, t, J=5.4Hz), 5.86 (IH, q, J=7.0Hz), 2.62 (3H, s), 2.00 (3H, d, J=7.0Hz). (K-12)
'H-NMR (CDC13) 6: 7.98 (IH, d, J=8.2Hz), 7.34 (2H, t, J=7.1Hz), 5.81 (IH, q, J=7.0Hz), 2.63 (3H, s), 2.01 (3H, d, J=7.0Hz).
Synthesis Example 47 (Starting material)
Figure imgf000087_0001
Sodium hydride (0.10 g) was added to a DMF solution (12 ml) of 4-methyl-5-pentafluoro- ethyl-4H-[l,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-(l,2,4)-triazole (0.55 g). 'H-NMR (CDCI3, ppm): 2.70 (3H, s), 3.80 (3H, s), 8.10-8.30 (3H, m).
Synthesis Example 48 (Starting material)
Figure imgf000087_0002
A mixture of 2-me ylmelcapto^.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). 'H-NMR (CDCI3, ppm): 3.48 (3H, s), 8.19 (IH, s). Synthesis Example 49 (Starting material)
Figure imgf000088_0001
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-bislrifluoromethyl-pyrimidine (1.03 g). 'H-NMR (CDC13, ppm): 2.60 (3H, s), 7.1-7.3 (2H, m), 7.67 (IH, s), 8.10 (IH, d). Synthesis Example 50 (Starting material)
Figure imgf000088_0002
(3-Methyl-4-mtrophenyl)-acetonitrile(3.52g) was dissolved in pyridine (30 ml), thereto excess H2S 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-phe- nyl)-thioacetamide (1.69 g). 'H-NMR (CDCI3, ppm): 2.60 (3H, s), 4.06 (2H, s), 6.40-8.00 (5H, m)
Synthesis Example 51 (Starting material)
Figure imgf000088_0003
2-(3-Methyl-4-nitrophenyl)-1hioacetamide (1.00 g), l-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-penta- fluoro-2-oxo-butyl ester (1.30 g). 'H-NMR (CDCI3, ppm): 2.55 (3H, s), 3.57 (2H, dd), 3.90 (2H, d), 7.24-7.22 (2H, m), 7.91-7.89 (IH, m) Synthesis Example 52 (Starting material)
Figure imgf000089_0001
Trifluoroacetic ar-hydride(1.47g) 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). 'H-NMR (CDC13, ppm): 2.63 (3H, s), 4.43 (2H, s), 7.30-7.28 (2H, m), 7.75 (IH, s), 7.98 (IH, d) 0 Synthesis Example 53 (Starting material)
Figure imgf000089_0002
An acetonitrile solution (20 ml) of 3-pentafluoroethyl-lH-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 of5 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-1 H-pyrazole (3.2 g). 'H-NMR (CDCI3, ppm): 7.77 (IH, s), 11.11(1H, m)
Synthesis Example 54 (Starting material)
Figure imgf000089_0003
4-Iodo-3-pentafluoroethyl-lH-pyrazole (6.24 g), copper powder (3.81 g), Iodo-l,l,2,2-tetrafluoro- ethane (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 '5 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-(l,l,2,2-tetrafluoroethyl)-lH-pyrazole (0.60 g), bp. 125-135°C/20 mbar. 'H-NMR (CDCI3, ppm): 5.98 (IH, tt), 7.96 (IH, s), 12.22 (IH, m) Synthesis Example 55 (Starting material)
Figure imgf000090_0001
4-Iodo-3-pentafluoroethyl-lH-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-lH-pyrazole (1.20 g), bp. 110-115°C/20 mbar. 'H-NMR (CDC13, ppm): 7.99 (IH, s), 12.31 (IH, m).
Synthesis Example 56 (Starting material)
Figure imgf000090_0002
An acetonitrile solution (20 ml) of 4-methyl-lH-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- lH-pyrazole (1.2 g). 'H-NMR (CDCI3, ppm): 2.03 (3H, s), 6.96 (IH, br s)
Synthesis Example 57 (Starting material)
Figure imgf000090_0003
5-Trifluoromethyl-lH-(l,2,4)-triazole-3-thiol(1.0g), heptafluoro-1-iodopropane (3.5 g) and triethylamine (0.90 g) were stirred in DMF (1 ml) at 90°C for 24 hours. After cooling to room temperature, he 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-trifluoro- methyl-lH-(l,2,4)-triazole (0.70g). Use examples
Biological Test Example 1: Test against larva of Spodoptera litura Preparation of test solution: Solvent: Dimethylformamide : 3 parts by weight
Emulsifier: 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 Guetiee 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 1/3 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)
15 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)
20 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.

Claims

Patent Claims
Novel benzenedicarboxamides of the formula (I)
Figure imgf000094_0001
wherein X represents hydrogen, halogen atom, nitro, Cι-6alkylsulfonyloxy, C_-6alkylsulfinyl, Cι-6alkylsulfenyl or Cι-6alkylsulfonyl, R' represents Cμ6alkyl, Cι-6alkylthio-Cι-6alkyl, Ci-6alkylsulfinyl-Ci-6alkyl or -βalkyl- sulfonyl-Cι_6alkyl, Y represents halogen or Cι_6alkyl, m represents 0 or 1, A represents O, S, SO, S02, CH2 or CH(CH3), and Q represents 5-membered 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.
2. The compounds of the formula (I) according to claim 1 wherein X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, Cι-_t alkylsulfonyloxy,
Figure imgf000094_0002
CM alkylsulfenyl or C1 alkylslfonyl, R1 represents
Figure imgf000094_0003
or Cι- alkyl- sulfonyl-Cι-4alkyl, Y represents fluorine, chlorine, bromine or Q^alkyl, m represents 0 or 1, A represents O, S, SO, SO2, CH2 or CH(CH3), and Q 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 Cι-6alkyl, Cι_6alkoxy, Cι-6alkylthio, Cι-6alkylsulfinyl, Cι-6alkylsulfonyl, -iohaloalkyl, -β haloalkoxy, Ci-βhaloalkylthio, Q-βhaloalkylsulfinyl, -6haloalkylsulfonyl, C].6 haloalkylcarbonyl, halogen, oxo and hydroxy group. The compounds of the formula (I) according to claim 1 wherein
X represents hydrogen, fluorine, chlorine, bromine, iodine, nitro, methanesulfonyloxy, C!-2 alkylsulfinyl, -2 alkylsulfenyl or -2 alkylslfonyl, R' represents isopropyl, Cι-2alkylthio-C3^alkyl, Cι-2alkylsulfinyl-C3-4alkyl or C.-2alkyl- sulfonyl-Cs^alkyl,
Y represents fluorine, chlorine or methyl, m represents 0 or 1,
A represents O, S, SO, S02, CH2 or CH(CH3), and
Q 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
Figure imgf000095_0001
Figure imgf000095_0002
alkoxy, Cι-4haloalkylthio, Cjjtialoalkylsulfinyl,
Figure imgf000095_0003
Cι-4haloalkyl- carbonyl, fluorine, chlorine, bromine, iodine, oxo and hydroxy group.
Processes for the preparation of the compounds of the formula (I) according to claim 1, characterized in that
(a) compounds of the formula (H)
Figure imgf000095_0004
wherein R and X have the same definition as in claim 1, are reacted with compounds of the formula (ID)
Figure imgf000095_0005
wherein Y, A, m and Q have the same definition as in claim 1 , in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or
(b) compounds of the formula (IV)
Figure imgf000095_0006
wherein X, Y, A, m and Q have the same definitions as in claim 1, are reacted with compounds of the formula (V) H2N-R1 • (V) wherein R1 has the same definition as in claim 1, in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or
(c) compounds of the formula (VI)
Figure imgf000096_0001
wherein X and R' have the same definitions as in claim 1, are reacted with the compounds of the formula (HI),
Figure imgf000096_0002
wherem Y, A, m and Q have the same definition as in claim 1 , in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or
(d) compounds of the formula (NO)
Figure imgf000096_0003
wherein X, Y, A, m and Q have the same definitions as in claim 1 , are reacted with the compounds of the formula (V), H2Ν-R1 (V) wherein R1 has the same definitions as in claim 1, in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or
(e) compounds of the formula (VET)
Figure imgf000097_0001
wherein X, Y, A, m and Q have the same definitions as in claim 1, are reacted with the compounds of the formula (V), H2N-R1 (V) wherein R1 has the same definitions as in claim 1, in the presence of inert solvents, and if appropriate in the presence of an acid catalyst, or (f) in case where R1 represents Cι-6alkylsulfinyl-Cι-6alkyl or Cι-6alkylsulfonyl-Cι-6alkyl in the formula (I): compounds of the formula (If)
Figure imgf000097_0002
wherein Rlf represents Cι-6alkylthio-Cι-6alkyl, and X, Y, A, m and Q have the same definitions as in claim 1, are reacted with an oxidizing agent in the presence of inert solvents.
Insecticidal compositions characterized in that they contain at least one of benzenedicarboxamides of the formula (I).
6. Process for controlling insects characterized in that benzenedicarboxamides of the formula (I) are allowed to act on insects and/or their habitat.
7. Use of benzenedicarboxamides of the formula (I) for controlling insects.
8. Process for the preparation of insecticidal compositions characterized in that benzene- dicarboxamides of the formula (I) are mixed with extenders and/or surface active agents. Novel compounds of the formula (IV)
Figure imgf000098_0001
wherein X, Y, A, m and Q have the same definitions as in claim 1.
10. Novel compounds of the formula (VH)
Figure imgf000098_0002
wherein X, Y, A, m and Q have the same definitions as in claim 1.
11. Novel compounds of the formula (VDI)
Figure imgf000098_0003
wherein X, Y, A, m and Q have the same definitions as aforementioned.
12. Novel compounds of the formula (K)
Figure imgf000098_0004
wherein Y, A, m and Q have the same definitions as in claim 1.
PCT/EP2005/002130 2004-03-12 2005-03-01 N1 - ((pyrazol-1-ymethyl) -2-methylphenyl)- phatalamide derivatives and related compounds insecticides WO2005095351A1 (en)

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KR101166122B1 (en) 2012-07-27
US20100130743A1 (en) 2010-05-27
JP5336074B2 (en) 2013-11-06
JP2006076990A (en) 2006-03-23
AU2005229339A1 (en) 2005-10-13
TWI350143B (en) 2011-10-11
KR20070026449A (en) 2007-03-08
EP1727804A1 (en) 2006-12-06
ATE447556T1 (en) 2009-11-15

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