WO2013187422A1 - Composition anti-organismes nuisibles utilisable dans le cadre de la lutte contre les arthropodes nuisibles et procédé de lutte contre les arthropodes nuisibles - Google Patents

Composition anti-organismes nuisibles utilisable dans le cadre de la lutte contre les arthropodes nuisibles et procédé de lutte contre les arthropodes nuisibles Download PDF

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WO2013187422A1
WO2013187422A1 PCT/JP2013/066126 JP2013066126W WO2013187422A1 WO 2013187422 A1 WO2013187422 A1 WO 2013187422A1 JP 2013066126 W JP2013066126 W JP 2013066126W WO 2013187422 A1 WO2013187422 A1 WO 2013187422A1
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group
compound
reaction
usually
condensed heterocyclic
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竜也 鈴木
岩田　淳
吉彦 野倉
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住友化学株式会社
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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
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • 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
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • 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
    • 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
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D263/57—Aryl or substituted aryl radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Definitions

  • the present invention relates to a harmful arthropod control composition and a method for controlling harmful arthropods.
  • Non-Patent Document 1 discloses many compounds as active ingredients of harmful arthropod control compositions.
  • An object of the present invention is to provide a harmful arthropod control composition having an excellent control effect on harmful arthropods.
  • A1 represents -NR6-, an oxygen atom or a sulfur atom
  • R 1, R 2, R 3 and R 4 are the same or different and each have one or more atoms or groups selected from C1-C3 chain hydrocarbon group optionally having one or more halogen atoms and group Z
  • R5 represents a C1-C3 chain hydrocarbon group which may have one or more atoms or groups selected from group X, -OR7, -S (O) mR7, or a halogen atom
  • R6 is a C1
  • -C6 represents an alicyclic hydrocarbon group or a hydrogen atom
  • R7 represents a C1-C3 chain hydrocarbon group which may have one or more halogen atoms or a hydrogen atom
  • m represents 0, 1 or 2
  • n represents 0, 1 or 2.
  • m represents 0, 1 or 2
  • R7 does not represent a hydrogen atom.
  • Group X C1-C3 alkoxy group optionally having one or more halogen atoms, C2-C3 alkenyloxy group optionally having one or more halogen atoms, having one or more halogen atoms
  • An optionally substituted C2-C3 alkynyloxy group, a C1-C3 alkylsulfanyl group optionally having one or more halogen atoms, a C1-C3 alkylsulfinyl optionally having one or more halogen atoms A group consisting of a group, a C1-C3 alkylsulfonyl group optionally having one or more halogen atoms, a cyano group, a hydroxy group, and a halogen atom;
  • Group Z C1-C3 chain hydrocarbon group optionally having one or more halogen atoms, C1-C3 alkoxy group optionally having one or more halogen atoms, one or more halogen atoms A C
  • Group W C1-C3 alkoxy group optionally having one or more halogen atoms, C2-C3 alkenyloxy group optionally having one or more halogen atoms, having one or more halogen atoms A group consisting of a C2-C3 alkynyloxy group, a halogen atom and a hydroxy group, which may be ]
  • a compound represented by Formula (2) [Where, R1 represents a hydrogen atom or a methyl group, R2 represents a methyl group, a difluoromethyl group or a trifluoromethyl group. ]
  • a harmful arthropod control composition comprising a compound represented by the formula:
  • -C6 represents an alicyclic hydrocarbon group or a hydrogen atom
  • R7 represents a C1-C3 chain hydrocarbon group which may have one or more halogen atoms or a hydrogen atom
  • m represents 0, 1 or 2
  • n represents 0, 1 or 2.
  • m represents 0, 1 or 2
  • R7 does not represent a hydrogen atom.
  • Group X C1-C3 alkoxy group optionally having one or more halogen atoms, C2-C3 alkenyloxy group optionally having one or more halogen atoms, having one or more halogen atoms
  • An optionally substituted C2-C3 alkynyloxy group, a C1-C3 alkylsulfanyl group optionally having one or more halogen atoms, a C1-C3 alkylsulfinyl optionally having one or more halogen atoms A group consisting of a group, a C1-C3 alkylsulfonyl group optionally having one or more halogen atoms, a cyano group, a hydroxy group, and a halogen atom;
  • Group Z C1-C3 chain hydrocarbon group optionally having one or more halogen atoms, C1-C3 alkoxy group optionally having one or more halogen atoms, one or more halogen atoms A C
  • Group W C1-C3 alkoxy group optionally having one or more halogen atoms, C2-C3 alkenyloxy group optionally having one or more halogen atoms, having one or more halogen atoms
  • a condensed heterocyclic compound represented by the following (hereinafter referred to as the present condensed heterocyclic compound); Formula (2) [Where, R1 represents a hydrogen atom or a methyl group, R2 represents a methyl group, a difluoromethyl group or a trifluoromethyl group. ] (Hereinafter referred to as the present carboxamide compound).
  • C1-C3 chain hydrocarbon group represents a linear or branched saturated or unsaturated hydrocarbon group having 1 to 3 carbon atoms, such as a methyl group, C1-C3 alkyl groups such as ethyl group, propyl group and isopropyl group; C2-C3 alkenyl groups such as vinyl group, 1-propenyl group, 2-propenyl group and 1-methylvinyl group; ethynyl group, propargyl group, 2- A C2-C3 alkynyl group such as a butynyl group may be mentioned.
  • C1-C2 chain hydrocarbon group represents a methyl group, an ethyl group, a vinyl group, or an ethynyl group.
  • C1-C3 alkyl group represents a linear or branched alkyl group having 1 to 3 carbon atoms, for example, a methyl group, an ethyl group, a propyl group, an isopropyl group. Is mentioned.
  • C1-C2 alkyl group represents a methyl group or an ethyl group.
  • C2-C3 alkenyl group is linear or branched having 2 to 3 carbon atoms, and has one or more double bonds in the molecule.
  • C2-C3 alkynyl group refers to a linear or branched chain having 2 to 3 carbon atoms and having one or more triple bonds in the molecule.
  • a saturated hydrocarbon group is represented, and examples thereof include an ethynyl group and a propargyl group.
  • C1-C3 alkoxy group represents a group represented by a linear or branched alkyl-O— having 1 to 3 carbon atoms, such as a methoxy group or an ethoxy group. , A propyloxy group, and an isopropyloxy group.
  • C2-C3 alkenyloxy group refers to a linear or branched chain having 2 to 3 carbon atoms, and one or more double bonds in the molecule. Represents a group represented by alkenyl-O-, and examples thereof include a vinyloxy group, a 1-propenyloxy group, a 2-propenyloxy group, and a 1-methylvinyloxy group.
  • C2-C3 alkynyloxy group is linear or branched having 2 to 3 carbon atoms, and has one or more triple bonds in the molecule. It represents a group represented by alkynyl-O—, and examples thereof include an ethynyloxy group and a propargyloxy group.
  • C1-C3 alkylsulfanyl group represents a group represented by linear or branched alkyl-S— having 1 to 3 carbon atoms, such as a methylsulfanyl group, Examples thereof include an ethylsulfanyl group, a propylsulfanyl group, and an isopropylsulfanyl group.
  • C1-C3 alkylsulfinyl group represents a group represented by linear or branched alkyl-S (O) — having 1 to 3 carbon atoms, such as methyl Examples thereof include a sulfinyl group, an ethylsulfinyl group, a propylsulfinyl group, and an isopropylsulfinyl group.
  • C1-C3 alkylsulfonyl group represents a group represented by a linear or branched alkyl-S (O) 2- having 1 to 3 carbon atoms, for example, Examples include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, and an isopropylsulfonyl group.
  • C3-C6 alicyclic hydrocarbon group represents a cyclic non-aromatic hydrocarbon group having 3 to 6 carbon atoms, such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, C3-C6 cycloalkyl group such as cyclohexyl group; C3-C6 cycloalkenyl group such as cyclopropenyl group, cyclobutenyl group, cyclopentenyl group, cyclohexenyl group and the like can be mentioned.
  • C3-C6 cycloalkyl group represents a cyclic alkyl group having 3 to 6 carbon atoms, and examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group.
  • the expression “may have one or more atoms or groups selected from group X” means that when it has two or more atoms or groups selected from group X, The atoms or groups selected from group X may be the same as or different from each other.
  • the expression “may have one or more atoms or groups selected from group Z” means that when it has two or more atoms or groups selected from group Z, The atoms or groups selected from group Z may be the same as or different from each other.
  • the expression “may have one or more atoms or groups selected from group W” means that when it has two or more atoms or groups selected from group W, those The atoms or groups selected from group W may be the same as or different from each other.
  • the expression “which may have one or more halogen atoms” means that when two or more halogen atoms are present, the halogen atoms may be the same as or different from each other. May be.
  • 6-membered heterocyclic group refers to a 6-membered heterocyclic compound containing one or more atoms selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom in addition to the carbon atom in the ring structure. Represents a residue, and examples thereof include a 6-membered aromatic heterocyclic group and a 6-membered non-aromatic heterocyclic group.
  • the “6-membered aromatic heterocyclic group” include a pyrazinyl group, a pyrimidinyl group, a pyridyl group, and a pyridazinyl group.
  • Examples of the “6-membered non-aromatic heterocyclic group” include a piperidyl group, a morpholinyl group, a piperazinyl group, and a thiomorpholinyl group.
  • halogen atom means a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
  • examples of the “C1-C3 chain hydrocarbon group optionally having one or more atoms or groups selected from group X” include a methyl group, an ethyl group, a propyl group, and an isopropyl group.
  • examples of the “C1-C3 chain hydrocarbon group optionally having one or more halogen atoms” include a methyl group, an ethyl group, a propyl group, an isopropyl group, a trifluoromethyl group, It has one or more halogen atoms such as trichloromethyl group, 2-fluoroethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, pentafluoroethyl group, heptafluoroisopropyl group, etc.
  • C1-C3 alkyl group C2-C3 alkenyl optionally having one or more halogen atoms such as vinyl group, 1-propenyl group, 2-propenyl group, 1-methylvinyl group, 1,1-difluoroallyl group and pentafluoroallyl group Group;
  • Examples include C2-C3 alkynyl group which may have one or more halogen atoms of ethynyl group and propargyl group.
  • Examples of the “C1-C3 alkyl group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a methyl group, an ethyl group, a propyl group, an isopropyl group, a trifluoromethyl group, and a trichloromethyl group. 2-fluoroethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, pentafluoroethyl group, heptafluoroisopropyl group and the like.
  • examples of the “phenyl group optionally having one or more atoms or groups selected from group Z” include a phenyl group, a 2-fluorophenyl group, a 3-fluorophenyl group, 4- Fluorophenyl group, 2,3-difluorophenyl group, 2,4-difluorophenyl group, 2,5-difluorophenyl group, 2,6-difluorophenyl group, 3,4-difluorophenyl group, 3,5-difluorophenyl Group, 2,3,4,5,6-pentafluorophenyl group, 2-chlorophenyl group, 3-chlorophenyl group, 4-chlorophenyl group, 2-bromophenyl group, 3-bromophenyl group, 4-bromophenyl group, 2-iodophenyl group, 3-iodophenyl group, 4-iodophenyl group, 2-trifluorophenyl group, 2-tri
  • examples of the “6-membered heterocyclic group optionally having one or more atoms or groups selected from group Z” include group Z such as piperidyl group, morpholyl group, and thiomorpholyl group.
  • a 6-membered non-aromatic heterocyclic group optionally having one or more atoms or groups selected from; Pyrazinyl group, 2-pyrimidinyl group, 4-pyrimidinyl group, 5-pyrimidinyl group, 2-pyridyl group, 3-pyridyl group, 4-pyridyl group, 3-fluoro-2-pyridyl group, 4-fluoro-2-pyridyl group , 5-fluoro-2-pyridyl group, 6-fluoro-2-pyridyl group, 2-pyrimidinyl group, 4-trifluoromethylpyridin-2-yl group, 5-trifluoromethylpyridin-2-yl group, etc.
  • Examples thereof include a 6-membered aromatic heterocyclic group which may have one or more atoms or groups selected from Z.
  • examples of the “C1-C3 chain hydrocarbon group optionally having one or more atoms or groups selected from group W” include a methyl group, an ethyl group, a propyl group, and an isopropyl group.
  • Trifluoromethyl group Trifluoromethyl group, trichloromethyl group, 2-fluoroethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, pentafluoroethyl group, methoxymethyl group, ethoxymethyl group, propyloxy Group W such as methyl group, isopropyloxymethyl group, methoxyethyl group, ethoxyethyl group, propyloxyethyl group, isopropyloxyethyl group, methylsulfanylethyl group, ethylsulfanylethyl group, methylsulfinylethyl group, and methylsulfonylethyl group Having one or more atoms or groups selected from And it may be C1-C3 alkyl group; C2-C3 alkenyl which may have one or more atoms or groups selected from the group W such as vinyl group, 1-prop
  • C3-C6 alicyclic hydrocarbon group optionally having one or more atoms or groups selected from group W includes cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl Group, cyclopropenyl group, cyclobutenyl group, cyclopentenyl group, 1-cyclohexenyl group, 2-cyclohexenyl group and 3-cyclohexenyl group.
  • Examples of the “C1-C3 alkylsulfanyl group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a methylsulfanyl group, an ethylsulfanyl group, a propylsulfanyl group, an isopropylsulfanyl group, and trifluoromethyl. Examples thereof include a sulfanyl group, a 2,2,2-trifluoroethylsulfanyl group, and a pentafluoroethylsulfanyl group.
  • Examples of the “C1-C3 alkylsulfinyl group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a methylsulfinyl group, an ethylsulfinyl group, a propylsulfinyl group, an isopropylsulfinyl group, and trifluoromethyl. Examples thereof include a sulfinyl group, a 2,2,2-trifluoroethylsulfinyl group and a pentafluoroethylsulfinyl group.
  • Examples of the “C1-C3 alkylsulfonyl group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, and trifluoromethyl. Examples include a sulfonyl group, a 2,2,2-trifluoroethylsulfonyl group, and a pentafluoroethylsulfonyl group.
  • Examples of the “C1-C3 alkoxy group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a methoxy group, a trifluoromethoxy group, an ethoxy group, and 2,2,2-trifluoroethoxy. Group, propyloxy group and isopropyloxy group.
  • examples of the “C2-C3 alkenyloxy group optionally having one or more halogen atoms” include 2-propenyloxy group, 2-methyl-2-propenyloxy group, 3, 3 -A difluoroallyloxy group and a 3, 3- dichloroallyloxy group are mentioned.
  • Examples of the “C2-C3 alkynyloxy group optionally having one or more halogen atoms” in the present condensed heterocyclic compound include a propargyloxy group.
  • one or more means one or more and the maximum number to which atoms or groups can be bonded, unless otherwise specified.
  • Examples of the present condensed heterocyclic compound include the following compounds.
  • A1 is -NR6-, an oxygen atom or a sulfur atom
  • R5 is a C1-C3 having one C1-C3 alkoxy group which may have one or more halogen atoms.
  • a chain hydrocarbon group a compound which is a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms;
  • A1 is —NR6-, an oxygen atom or a sulfur atom, A2 is N, and R5 has one C1-C3 alkoxy group which may have one or more halogen atoms.
  • a C1-C3 chain hydrocarbon group a compound which is a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms;
  • A1 is -NR6-, an oxygen atom or a sulfur atom
  • R5 is a C1-C3 having one C1-C3 alkoxy group which may have one or more halogen atoms.
  • A1 is —NR 6 — or a sulfur atom
  • R 5 is a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms
  • R 6 is a methyl group ;
  • A1 is —NR6-, an oxygen atom or a sulfur atom
  • A2 is N
  • R5 has one C1-C3 alkoxy group which may have one or more halogen atoms.
  • a C1-C3 chain hydrocarbon group, a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms, and R6 is a methyl group;
  • A1 is -NR6- or a sulfur atom
  • A2 is N
  • R5 is a C1-C3 chain hydrocarbon group which may have one or more halogen atoms
  • R6 A compound wherein is a methyl group;
  • A1 is —NR6-
  • A2 is N
  • R5 is a C1-C2 chain hydrocarbon group optionally having one or more halogen atoms
  • R6 is a methyl group.
  • A1 is -NR6- or a sulfur atom
  • A2 is N
  • R5 is -S (O) mR7
  • R7 may have one or more halogen atoms.
  • A1 is -NR6- or a sulfur atom
  • R5 is -S (O) mR7
  • R6 is a methyl group
  • R7 may have one or more halogen atoms.
  • a compound which is a C1-C3 chain hydrocarbon group In Formula (1), A1 is —NR6- or a sulfur atom, A2 is N, R5 is —S (O) mR7, R6 is a methyl group, and R7 is one or more halogen atoms.
  • a compound which is a C1-C3 chain hydrocarbon group optionally having; In Formula (1), A1 is a sulfur atom, A2 is N, R5 is -S (O) mR7, R6 is a methyl group, and R7 has one or more halogen atoms.
  • R2, R3 and R4 are the same or different and each is a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms, -OR7, a halogen atom or a hydrogen atom, A compound wherein R5 is a C1-C3 chain hydrocarbon group optionally having one or more halogen atoms, -OR7, or a halogen atom; In the formula (1), R2, R3 and R4 are the same or different and may have one or more halogen atoms or a C1-C2 alkyl group which may have one or more halogen atoms.
  • R5 is a 6-membered heterocyclic group optionally having one or more halogen atoms or a C1-C2 alkyl group optionally having one or more halogen atoms.
  • R2, R3 and R4 are the same or different and are a fluorine atom, a chlorine atom, a bromine atom, an iodine atom or a hydrogen atom
  • R5 is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom
  • R2, R3 and R4 are the same or different and are a fluorine atom, a chlorine atom, a bromine atom, a methyl group, a trifluoromethyl group, a trifluoromethoxy group, a pentafluoroethyl group or a hydrogen atom
  • R5 A compound in which is a fluorine atom, a chlorine atom, a bromine atom, a methyl group, a trifluoromethyl group, a trifluoromethoxy group or a pentafluoroeth
  • A1A represents -NR6A-, an oxygen atom or a sulfur atom
  • R1A, R3A and R4A are the same or different and represent a halogen atom or a hydrogen atom (provided that at least two of R1A, R3A and R4A represent a hydrogen atom)
  • R2A is a C1-C3 alkyl group optionally having one or more halogen atoms, a C1-C3 alkoxy group optionally having one or more halogen atoms, and a C1-C3 having one or more halogen atoms.
  • a 6-membered aromatic heterocyclic group optionally having a C3 alkyl group, a halogen atom or a hydrogen atom
  • R5A represents a C1-C3 alkyl group optionally having one or more halogen atoms, or -S (O) mR7A
  • R6A represents a C1-C3 alkyl group or a C3-C6 cycloalkyl group
  • R7A represents a C1-C3 alkyl group optionally having one or more halogen atoms
  • m represents 0, 1 or 2
  • n represents 0, 1 or 2.
  • A1B represents -NR6B-, an oxygen atom or a sulfur atom
  • R1B, R3B and R4B are the same or different and represent a fluorine atom, a chlorine atom or a hydrogen atom (provided that at least two of R1B, R3B and R4B represent a hydrogen atom)
  • R2B is a C1-C3 alkyl group (particularly a methyl group, ethyl group or isopropyl group), a C1-C3 alkyl group having one or more halogen atoms (particularly a difluoromethyl group, a trifluoromethyl group, a pentafluoroethyl group, A heptafluoropropyl group, etc.) a C1-C3 alkoxy group having at least one halogen atom (especially a trifluoromethoxy group, etc.), a nitrogen-containing 6-
  • the compounds represented by the general formulas (1A) and (1B) are included in the condensed heterocyclic compound represented by the general formula (1).
  • the present condensed heterocyclic compound can be produced, for example, by the following (Production Method A) to (Production Method F).
  • This condensed heterocyclic compound (1) can be produced by reacting the compound (M1) with the compound (M2). Alternatively, it can be produced by reacting the compound (M1) and the compound (M2) to produce the compound (M3) and cyclizing the compound (M3). [Wherein, R 1, R 2, R 3, R 4, R 5, A 1, A 2 and n represent the same meaning as described above. ]
  • This condensed heterocyclic compound (1) can be produced by reacting the compound (M1) with the compound (M4). Alternatively, it can be produced by reacting the compound (M1) and the compound (M4) to produce the compound (M3) and cyclizing the compound (M3). [Wherein, R 1, R 2, R 3, R 4, R 5, A 1, A 2 and n represent the same meaning as described above. ]
  • This fused heterocyclic compound (1) can be produced by reacting compound (M1) with compound (M5). Alternatively, it can be produced by reacting the compound (M1) and the compound (M5) to produce the compound (M6) and cyclizing the compound (M6). [Wherein, R 1, R 2, R 3, R 4, R 5, A 1, A 2 and n represent the same meaning as described above. ]
  • the production methods (Production Method A) to (Production Method F) of the present condensed heterocyclic compound will be described in more detail below.
  • a production method from the present condensed heterocyclic compound to another condensed heterocyclic compound will be described.
  • the present condensed heterocyclic compound can be produced, for example, by the following (Production Method 1) to (Production Method 23).
  • Step (C-1) Compound (4) in which A1 is -NR6- in formula (1) can be produced by reacting compound (M12) and compound (M5) according to step (C-1).
  • R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above.
  • the reaction is usually carried out in the presence of a base, acid, sulfite or disulfite.
  • the reaction is usually performed in the presence of a solvent.
  • the base used in the reaction include hydrogen carbonates such as sodium hydrogen carbonate and potassium hydrogen carbonate, carbonates such as sodium carbonate and potassium carbonate, and mixtures thereof.
  • Examples of the acid used for the reaction include sulfonic acids such as p-toluenesulfonic acid and carboxylic acids such as acetic acid.
  • Examples of the sulfite used in the reaction include sodium sulfite and potassium sulfite.
  • Examples of the disulfite used in the reaction include sodium disulfite and potassium disulfite.
  • Examples of the solvent used in the reaction include ethers such as tetrahydrofuran (hereinafter referred to as THF), ethylene glycol dimethyl ether, tert-butyl methyl ether, 1,4-dioxane, and aliphatic hydrocarbons such as hexane, heptane, and octane.
  • Aromatic hydrocarbons such as toluene and xylene, halogenated hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, N, N-dimethylformamide (hereinafter referred to as DMF) ), Acid amides such as N-methylpyrrolidone (hereinafter referred to as NMP), sulfoxides such as dimethyl sulfoxide (hereinafter referred to as DMSO), nitrogen-containing aromatic compounds such as pyridine and quinoline, and the like. A mixture is mentioned.
  • the reaction can be carried out by adding an oxidizing agent as necessary.
  • the oxidizing agent used in the reaction examples include oxygen, copper (II) chloride, 2,3-dichloro-5,6-dicyano-p-benzoquinone, and the like.
  • the compound (M5) is usually 1 to 3 mol
  • the base is usually 1 to 5 mol
  • the acid is usually 1 to 5 mol
  • sulfite Is usually used in a proportion of 1 to 5 mol
  • disulfite is usually used in a proportion of 1 to 5 mol
  • oxidizing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (4) can be isolated by performing post-treatment operations such as adding water to the reaction mixture, extracting with an organic solvent, and drying and concentrating the organic layer.
  • the isolated compound (4) can be further purified by chromatography, recrystallization and the like.
  • Step A-1 Compound (4) in which A1 is —NR6- in formula (1) is produced by reacting compound (M12) and compound (M2) in the presence of a dehydration condensing agent according to step (A-1). can do. [Wherein, R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, tert-butyl methyl ether, ethylene glycol dimethyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Examples of the dehydrating condensing agent used in the reaction include 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride (hereinafter referred to as WSC), carbodiimides such as 1,3-dicyclohexylcarbodiimide, (benzotriazole- 1-yloxy) tris (dimethylamino) phosphonium hexafluorophosphate (hereinafter referred to as BOP reagent) and the like.
  • WSC 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride
  • carbodiimides such as 1,3-dicyclohexylcarbodiimide
  • BOP reagent benzotriazole- 1-yloxy tris (dimethylamino) phosphonium hexafluorophosphate
  • This reaction can also be performed by adding a catalyst as needed.
  • Examples of the catalyst used in the reaction include
  • the compound (M2) is usually in a proportion of 1 to 3 mol
  • the dehydrating condensing agent is usually in a proportion of 1 to 5 mol
  • the catalyst is usually in a proportion of 0.01 to 0.1. Used in molar proportions.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (4) can be isolated by performing post-treatment operations such as adding water to the reaction mixture, extracting with an organic solvent, and drying and concentrating the organic layer. The isolated compound (4) can be further purified by chromatography, recrystallization and the like.
  • the compound (M4) can be used instead of the compound (M2), and the compound (4) can be produced according to the above method.
  • the compound (M4) is usually carried out without adding a dehydrating condensation agent.
  • a base can be added as necessary.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol
  • the base is usually used in a proportion of 1 to 10 mol.
  • Step (A-3), Step (B-3) Compound (4) in which A1 is -NR6- in formula (1) can be produced by dehydrating condensation of compound (M13) according to step (A-3) or step (B-3). [Wherein, R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, methanol, ethanol, propanol , Alcohols such as butanol and pentanol, and mixtures thereof.
  • an acid or a dehydrating agent can be used as necessary.
  • the acid used in the reaction include sulfonic acids such as p-toluenesulfonic acid, and carboxylic acids such as acetic acid.
  • Examples of the dehydrating agent used in the reaction include phosphorus oxychloride, acetic anhydride, trifluoroacetic anhydride, and the like. Can be mentioned.
  • an acid or a dehydrating agent is usually used at a ratio of 1 mol to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (4) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (4) can be further purified by chromatography, recrystallization and the like.
  • Step (A-3), Step (B-3) Compound (4) in which A1 is -NR6- in formula (1) is produced by reacting compound (M13) in the presence of a base according to step (A-3) or step (B-3). Can do. [Wherein, R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • the base used for the reaction include tripotassium phosphate.
  • the base is generally used at a ratio of 1 mol to 10 mol with respect to 1 mol of the compound (M13).
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (4) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (4) can be further purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, DMF, Examples include acid amides such as NMP, sulfoxides such as DMSO, and mixtures thereof.
  • Examples of the base used in the reaction include alkali metal or alkaline earth metal hydrides such as sodium hydride, potassium hydride and calcium hydride, inorganic bases such as sodium carbonate and potassium carbonate, and organic bases such as triethylamine. Is mentioned.
  • compound (M14) is usually used at a ratio of 1 to 5 mol per 1 mol of compound (5).
  • the base is usually used at a ratio of 1 to 3 mol with respect to 1 mol of the compound (5).
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (4) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (4) can be further purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene. Group hydrocarbons, halogenated hydrocarbons such as chlorobenzene and dichlorobenzene, and mixtures thereof.
  • Examples of the acid used for the reaction include polyphosphoric acid and trimethylsilyl polyphosphate. The reaction is usually carried out without a solvent when polyphosphoric acid is used as the acid, but it may be carried out in a solvent.
  • the compound (M2) is usually used in a proportion of 1 to 3 mol, and the acid is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (6) can be isolated by performing post-treatment operations such as pouring the reaction mixture into water, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (6) can be further purified by chromatography, recrystallization and the like.
  • the compound (M4) can replace with a compound (M2) and can use a compound (M4) and can manufacture a compound (6) according to the said method according to a process (B-1).
  • the compound (M4) is usually carried out without adding a dehydrating condensation agent.
  • a base can be added as necessary.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol
  • the base is usually used in a proportion of 1 to 10 mol.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • the oxidizing agent is usually used at a ratio of 1 to 3 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (6) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (6) can be further purified by chromatography, recrystallization and the like.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, dichloromethane, chloroform, carbon tetrachloride, Examples thereof include halogenated hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, and mixtures thereof. Of these, carbon tetrachloride can also be used as a dehydrating condensing agent.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aromatic hydrocarbons such as toluene and xylene
  • dichloromethane chloroform
  • carbon tetrachloride examples thereof include halogenated hydro
  • Examples of the dehydrating condensing agent used in the reaction include a mixture of triphenylphosphine, a base, and carbon tetrachloride or carbon tetrabromide, a mixture of triphenylphosphine and an azodiester such as azodicarboxylic acid diethyl ester, and the like.
  • Examples of the base used in the reaction include tertiary amines such as triethylamine and diisopropylethylamine.
  • the dehydrating condensing agent is usually used at a ratio of 1 to 3 moles relative to 1 mole of the compound (M17).
  • the base When a base is used, the base is usually used at a ratio of 1 to 5 mol with respect to 1 mol of the compound (M17).
  • the reaction temperature is usually in the range of ⁇ 30 to 100 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (6) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (6) can be further purified by chromatography, recrystallization and the like.
  • Step (A-3), Step (B-3) Compound (6) in which A1 is an oxygen atom in formula (1) can be produced by reacting compound (M17) in the presence of an acid according to step (A-3) or step (B-3). It can. [Wherein, R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, and halogens such as dichloromethane, chloroform, and chlorobenzene. Hydrocarbons and mixtures thereof.
  • Examples of the acid include sulfonic acids such as p-toluenesulfonic acid, polyphosphoric acid, and the like. In the reaction, an acid is usually used at a ratio of 0.1 to 3 mol with respect to 1 mol of the compound (M17).
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 1 to 24 hours.
  • the compound (6) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (6) can be further purified by chromatography, recrystallization and the like.
  • Examples of the acid used for the reaction include sulfonic acids such as p-toluenesulfonic acid and carboxylic acids such as acetic acid.
  • Examples of the sulfite used in the reaction include sodium sulfite and potassium sulfite.
  • Examples of the disulfite used in the reaction include sodium disulfite and potassium disulfite. The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and halogenation such as chlorobenzene.
  • the reaction can be carried out by adding an oxidizing agent as necessary.
  • the oxidizing agent used in the reaction include oxygen, copper (II) chloride, 2,3-dichloro-5,6-dicyano-p-benzoquinone, and the like.
  • the compound (M5) is usually 1 to 3 moles
  • the base is 1 to 5 moles
  • the acid is usually 1 to 5 moles
  • the sulfite is added.
  • disulfite is usually used in 1 to 5 moles
  • oxidant is usually used in 1 to 5 moles.
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (2) can be isolated by performing post-treatment operations such as addition of the reaction mixture to water, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (2) can also be purified by chromatography, recrystallization and the like.
  • the compound (M5) is usually used at a ratio of 0.5 to 3 moles and the base is usually used at a ratio of 1 to 2 moles relative to 1 mole of the compound (M18).
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (2) can be isolated by performing post-treatment operations such as addition of the reaction mixture to water, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (2) can also be purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene. Group hydrocarbons, alcohols such as methanol and ethanol, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof.
  • Examples of the cyanating agent used in the reaction include zinc cyanide, and examples of the di (C1-C3 alkyl) zinc include dimethyl zinc, diethyl zinc, and diisopropyl zinc.
  • the palladium compound used for the reaction examples include tetrakis (triphenylphosphine) palladium.
  • the cyanating agent or di (C1-C3 alkyl) zinc is usually in a proportion of 1 to 5 mol
  • the palladium compound is usually in a proportion of 0.01 to 0.5 mol.
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (8) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (8) can be further purified by chromatography, recrystallization and the like.
  • the compound (M19) is usually used in a proportion of 1 to 10 mol, and copper iodide is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (9) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (9) can be further purified by chromatography, recrystallization and the like.
  • Nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof.
  • the base used for the reaction include alkali metal hydrides such as sodium hydride.
  • the reaction temperature of the reaction is usually in the range of 0 to 150 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (3) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (3) can be further purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, DMF, Examples include acid amides such as NMP, sulfoxides such as DMSO, and mixtures thereof.
  • Examples of the base used in the reaction include alkali metal or alkaline earth metal hydrides such as sodium hydride, potassium hydride and calcium hydride, inorganic bases such as sodium carbonate and potassium carbonate, and organic bases such as triethylamine. Can be mentioned.
  • the base is usually used at a ratio of 1 to 3 mol
  • the compound (M21) is usually used at a ratio of 1 to 3 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (3) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (3) can be further purified by chromatography, recrystallization and the like.
  • the oxidizing agent is used in a proportion of 1 to 1.2 mol with respect to 1 mol of the compound (3).
  • the reaction temperature is usually in the range of ⁇ 20 to 80 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite, sodium thiosulfate) or an aqueous solution of a base (for example, sodium bicarbonate) as necessary, dried,
  • a reducing agent for example, sodium sulfite, sodium thiosulfate
  • a base for example, sodium bicarbonate
  • an oxidizing agent is usually used in a ratio of 2 to 5 mol with respect to 1 mol of the compound (3).
  • the oxidizing agent is used in a ratio of 2 to 3 moles with respect to 1 mole of the compound (3).
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • Compound (11) can be isolated by performing post-treatment operations such as concentration.
  • the isolated compound (11) can be further purified by chromatography, recrystallization and the like.
  • the oxidizing agent is usually used at a ratio of 1 to 4 moles relative to 1 mole of the compound (10).
  • the oxidizing agent is used in a ratio of 1 to 2 moles relative to 1 mole of the compound (10).
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • Compound (11) can be isolated by performing post-treatment operations such as concentration.
  • the isolated compound (11) can be further purified by chromatography, recrystallization and the like.
  • Step (A-3), Step (B-3) Compound (2) in which A1 is a sulfur atom in formula (1) can be produced by reacting compound (M22) in the presence of an acid according to step (A-3) or step (B-3). It can. [Wherein, R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, and halogens such as dichloromethane, chloroform, and chlorobenzene. Hydrocarbons and mixtures thereof.
  • Examples of the acid used for the reaction include sulfonic acids such as p-toluenesulfonic acid and polyphosphoric acid. In the reaction, an acid is usually used at a ratio of 0.1 to 3 mol with respect to 1 mol of the compound (M22).
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 1 to 24 hours.
  • the compound (2) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (2) can be further purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include aromatic hydrocarbons such as toluene and xylene, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof.
  • Examples of the thiolating agent used in the reaction include sodium sulfide, sodium sulfide nonahydrate, and thiourea.
  • Examples of the catalyst used in the reaction include copper (I) chloride, copper (I) bromide, and copper (I) iodide. This reaction can also be performed in presence of a base as needed.
  • Examples of the base used in the reaction include potassium carbonate, cesium carbonate, tripotassium phosphate, and triethylamine.
  • the thiolating agent is usually used in a proportion of 1 to 10 mol
  • the catalyst is usually used in a proportion of 0.1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 50 to 200 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (12-a) and / or the compound (12-b) is isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. be able to.
  • the isolated compound (12-a) and / or compound (12-b) can be further purified by chromatography, recrystallization and the like.
  • Step (22-2) Compound (13) can be produced by reacting compound (12-a) and / or compound (12-b) with compound (M23) in the presence of a base.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include alcohols such as methanol and ethanol, ethers such as 1,4-dioxane, diethyl ether, THF and tert-butyl methyl ether, dichloromethane, chloroform, carbon tetrachloride, and 1,2.
  • -Halogenated hydrocarbons such as dichloroethane and chlorobenzene, aromatic hydrocarbons such as toluene, benzene and xylene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, DMF, NMP, 1,3-dimethyl
  • aprotic polar solvents such as 2-imidazolidinone and dimethyl sulfoxide
  • nitrogen-containing aromatic compounds such as pyridine and quinoline, water, and mixtures thereof.
  • Examples of the base used in the reaction include pyridine, picoline, 2,6-lutidine, diazabicycloundecene (hereinafter referred to as DBU), 1,5-diazabicyclo [4.3.0] -5-nonene, and the like. And nitrogen-containing heterocyclic compounds, tertiary amines such as triethylamine and N-ethyldiisopropylamine, and inorganic bases such as tripotassium phosphate, potassium carbonate, sodium hydride, sodium hydroxide and potassium hydroxide.
  • DBU diazabicycloundecene
  • the compound (M23) is usually used at a ratio of 1 to 10 mol and the base is usually used at a ratio of 1 to 5 mol. It is done.
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (13) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (13) can be further purified by chromatography, recrystallization and the like.
  • Step (22-3) In compound (14), a compound in which m is 1 or 2 can be produced by subjecting compound (13) to an oxidation reaction.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include halogenated hydrocarbons such as dichloromethane and chloroform, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used in the reaction include m-chloroperbenzoic acid or hydrogen peroxide water.
  • the reaction can be carried out in the presence of a catalyst as necessary. Examples of the catalyst used for the reaction include sodium tungstate.
  • the oxidizing agent is usually used at a ratio of 1 to 5 moles.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite, sodium thiosulfate) or an aqueous solution of a base (for example, sodium bicarbonate) as necessary, dried,
  • a reducing agent for example, sodium sulfite, sodium thiosulfate
  • a base for example, sodium bicarbonate
  • the compound (15) in which R5 is —OR7 can be produced, for example, by the following method.
  • R1, R2, R3, R4, R7, A1, A2, V1 and n represent the same meaning as described above.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, DMF, Examples include acid amides such as NMP, sulfoxides such as DMSO, and mixtures thereof.
  • Examples of the base used in the reaction include alkali metal or alkaline earth metal hydrides such as sodium hydride, potassium hydride and calcium hydride, inorganic bases such as sodium carbonate, potassium carbonate and cesium carbonate, or triethylamine. An organic base is mentioned.
  • This reaction can also be performed by adding a copper compound as necessary.
  • Examples of the copper compound used in the reaction include copper, copper (I) iodide, copper (I) bromide, and copper (I) chloride.
  • the compound (M24) is usually used in a proportion of 1 to 5 mol and the base is usually used in a proportion of 1 to 3 mol with respect to 1 mol of the compound (7).
  • the reaction temperature of the reaction is usually in the range of 20 to 250 ° C.
  • the reaction time is usually in the range of 0.1 to 48 hours.
  • the reaction mixture is poured into water and then extracted with an organic solvent, and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture
  • the collected solid can be collected by filtration to isolate compound (15).
  • the isolated compound (15) can be further purified by recrystallization, chromatography or the like.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, BOP reagent and the like. This reaction can also be performed by adding a catalyst as needed. Examples of the catalyst used for the reaction include HOBt.
  • the compound (M2) is usually in a ratio of 1 to 3 moles
  • the dehydration condensing agent is usually in a ratio of 1 to 5 moles
  • the catalyst is usually in a range of 0.01 to 0.1 Used in molar proportions.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (2) can be isolated by performing post-treatment operations such as adding water to the reaction mixture, extracting with an organic solvent, and drying and concentrating the organic layer. The isolated compound (2) can be further purified by chromatography, recrystallization and the like.
  • the compound (M4) can replace with a compound (M2) and can use a compound (M4) and can manufacture a compound (2) according to the said method according to a process (B-1).
  • the compound (M4) is usually carried out without adding a dehydrating condensation agent.
  • a base can be added as necessary.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol
  • the base is usually used in a proportion of 1 to 10 mol.
  • Examples of the solvent used in the reaction include ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran, tert-butyl methyl ether, and diglyme, and halogenations such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, and chlorobenzene.
  • ethers such as 1,4-dioxane, diethyl ether, tetrahydrofuran, tert-butyl methyl ether, and diglyme
  • halogenations such as dichloromethane, chloroform, carbon tetrachloride, 1,2-dichloroethane, and chlorobenzene.
  • Examples thereof include hydrocarbons, hydrocarbons such as toluene, benzene and xylene, nitriles such as acetonitrile, pyridines such as pyridine, picoline and lutid
  • Examples of the sulfurizing agent used in the reaction include nilin pentasulfide, Lawesson's reagent (2,4-bis- (4-methoxyphenyl) -1,3-dithia-2,4-diphosphetan-2,4-disulfide) and the like. Can be mentioned.
  • the amount of the sulfiding agent used for the reaction is usually 1 mol or more per 1 mol of the compound (M7).
  • the reaction temperature of the reaction is usually in the range of 0 ° C. to 200 ° C., and the reaction time is usually in the range of 1 to 24 hours.
  • reaction mixture After completion of the reaction, the reaction mixture is poured into water and then extracted with an organic solvent, and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture
  • the collected solid can be collected by filtration to isolate compound (2).
  • the isolated compound (2) can be further purified by recrystallization, chromatography or the like.
  • the intermediate of the present invention can be produced, for example, by the following method.
  • Compound (M12) can be produced by the following method. [Wherein R5, R6 and A2 represent the same meaning as described above. ]
  • Compound (M26) can be produced by reacting compound (M25) in the presence of a nitrating agent. The reaction is usually performed in the presence of a solvent. Examples of the solvent used in the reaction include halogenated hydrocarbons such as dichloromethane and chloroform, acetic acid, concentrated sulfuric acid, concentrated nitric acid, water, and mixtures thereof. An example of the nitrating agent used in the reaction is concentrated nitric acid.
  • the nitrating agent is usually used at a ratio of 1 to 3 moles relative to 1 mole of the compound (M25).
  • the reaction temperature is usually in the range of ⁇ 10 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M26) can be isolated by performing post-treatment operations such as pouring the reaction mixture into water, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M26) can be further purified by chromatography, recrystallization and the like.
  • Compound (M12) can be produced by reacting compound (M26) with hydrogen in the presence of a hydrogenation catalyst.
  • the reaction is usually performed in the presence of a solvent under a hydrogen atmosphere of 1 to 100 atm.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether and 1,4-dioxane, esters such as ethyl acetate and butyl acetate, alcohols such as methanol and ethanol, water And mixtures thereof.
  • the hydrogenation catalyst used in the reaction include transition metal compounds such as palladium carbon, palladium hydroxide, Raney nickel, and platinum oxide.
  • the reaction with respect to 1 mole of the compound (M26), hydrogen is usually used at a ratio of 3 moles, and the hydrogenation catalyst is usually used at a ratio of 0.001 to 0.5 moles.
  • This reaction can also be carried out by adding an acid (such as a base) as necessary.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M12) can be isolated by performing post-treatment operations such as filtration of the reaction mixture, extraction with an organic solvent, if necessary, and drying and concentration of the organic layer.
  • the isolated compound (M12) can be further purified by chromatography, recrystallization and the like.
  • Step (A-2) Compound (M13) can be produced by reacting compound (M12) and compound (M2) in the presence of a dehydration condensing agent according to step (A-2). [Wherein, R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, and BOP reagent.
  • the compound (M2) is usually used in a proportion of 1 to 3 mol, and the dehydrating condensing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 140 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M13) can be isolated by performing post-treatment operations such as water addition to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M13) can be further purified by chromatography, recrystallization and the like.
  • Step (B-2) Compound (M13) can be produced by reacting compound (M12) and compound (M4) in the presence of a base according to step (B-2).
  • a base a base
  • R 1, R 2, R 3, R 4, R 5, R 6, A 2 and n represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Aromatic hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof It is done.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M13) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M13) can be further purified by chromatography, recrystallization and the like.
  • Compound (M15) can be produced by the following method. [Wherein R5 and A2 represent the same meaning as described above. ]
  • Compound (M28) can be produced by reacting compound (M27) in the presence of a nitrating agent. The reaction is usually performed in the presence of a solvent. Examples of the solvent used in the reaction include aliphatic halogenated hydrocarbons such as chloroform, acetic acid, concentrated sulfuric acid, concentrated nitric acid, water, and mixtures thereof. An example of the nitrating agent used in the reaction is concentrated nitric acid.
  • the nitrating agent is usually used at a ratio of 1 to 3 moles relative to 1 mole of the compound (M27).
  • the reaction temperature is usually in the range of ⁇ 10 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M28) can be isolated by performing post-treatment operations such as pouring the reaction mixture into water, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M28) can be further purified by chromatography, recrystallization and the like.
  • Compound (M15) can be produced by reacting compound (M28) with hydrogen in the presence of a hydrogenation catalyst.
  • the reaction is usually performed in the presence of a solvent under a hydrogen atmosphere of 1 to 100 atm.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether and 1,4-dioxane, esters such as ethyl acetate and butyl acetate, alcohols such as methanol and ethanol, water And mixtures thereof.
  • the hydrogenation catalyst used in the reaction include transition metal compounds such as palladium carbon, palladium hydroxide, Raney nickel, and platinum oxide.
  • the reaction hydrogen is usually used in a proportion of 3 mol and a hydrogenation catalyst is usually used in a proportion of 0.001 to 0.5 mol with respect to 1 mol of the compound (M28).
  • This reaction can also be carried out by adding an acid (such as a base) as necessary.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M15) can be isolated by performing post-treatment operations such as filtration of the reaction mixture, extraction with an organic solvent, if necessary, and drying and concentration of the organic layer.
  • the isolated compound (M15) can be further purified by chromatography, recrystallization and the like.
  • Step (C-2) Compound (M16) can be produced by reacting compound (M15) with compound (M5) according to step (C-2).
  • R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include alcohols such as methanol and ethanol, ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, and the like. These mixtures are mentioned.
  • compound (M5) is generally used at a ratio of 1 to 3 mol per 1 mol of compound (M15).
  • This reaction can also be performed by adding an acid, a base, or the like, if necessary.
  • the reaction temperature of the reaction is usually in the range of 0 to 150 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M16) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, drying and concentration. The isolated compound (M16) can be further purified by chromatography, recrystallization and the like.
  • Step (A-2) Compound (M17) can be produced by reacting compound (M15) and compound (M2) in the presence of a dehydration condensing agent according to step (A-2). [Wherein, R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, and BOP reagent.
  • the compound (M2) is usually used in a proportion of 1 to 3 mol, and the dehydrating condensing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 140 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M17) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M17) can be further purified by chromatography, recrystallization and the like.
  • Step (B-2) Compound (M17) can be produced by reacting compound (M15) and compound (M4) in the presence of a base according to step (B-2).
  • a base a base
  • R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Aromatic hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof It is done.
  • Examples of the base used in the reaction include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine. It is done.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M17) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M17) can be further purified by chromatography, recrystallization and the like.
  • Compound (M18) can be produced by the following method. [Wherein R5 and A2 represent the same meaning as described above. ]
  • Compound (M30) can be produced by reacting compound (M29) with thiourea in the presence of a base. The reaction is usually performed in the presence of a solvent. Examples of the solvent used in the reaction include alcohols such as methanol and ethanol, water, and mixtures thereof. Examples of the base used for the reaction include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide.
  • thiourea is usually used in a proportion of 0.5 to 3 mol
  • base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M30) can be isolated by performing post-treatment operations such as addition of an acid to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M30) can also be purified by chromatography, recrystallization, and the like.
  • Compound (M18) can be produced by subjecting compound (M30) to a reduction reaction.
  • the reduction reaction can be performed in the presence of a reducing agent such as iron powder or zinc powder; an acid such as hydrochloric acid or acetic acid; and water.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, esters such as ethyl acetate and butyl acetate, alcohols such as methanol and ethanol, Examples thereof include acid amides such as DMF and NMP, and mixtures thereof.
  • the reducing agent is usually used in a proportion of 3 to 10 mol per 1 mol of the compound (M30).
  • the reaction temperature is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M18) can be isolated by performing post-treatment operations such as addition of water to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M18) can also be purified by chromatography, recrystallization, and the like.
  • compound (M9) wherein A1 is -NR6- can be produced by reacting compound (M12) with compound (M31) in the presence of a base.
  • a base for reacting compound (M12) with compound (M31) in the presence of a base.
  • R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the base used in the reaction include hydrogen carbonates such as sodium hydrogen carbonate and potassium hydrogen carbonate, carbonates such as sodium carbonate and potassium carbonate, sulfites such as sodium sulfite and potassium sulfite, and mixtures thereof.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • the compound (M33) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M33) can be further purified by chromatography, recrystallization and the like.
  • Step (E-1) In compound (M10), compound (M33) wherein A1 is -NR6- is obtained by reacting compound (M12) and compound (M8) in the presence of a dehydration condensing agent according to step (E-1). Can be manufactured. [Wherein R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, tert-butyl methyl ether, ethylene glycol dimethyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, tert-butyl methyl ether, ethylene glycol dimethyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, BOP reagent and the like. This reaction can also be performed by adding a catalyst as needed. Examples of the catalyst used in the reaction include HOBt.
  • the compound (M8) is usually in a proportion of 1 to 3 mol
  • the dehydrating condensing agent is usually in a proportion of 1 to 5 mol
  • the catalyst is usually in a proportion of 0.01 to 0.1. Used in molar proportions.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M33) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M33) can be further purified by chromatography, recrystallization and the like.
  • Step (E-3) In compound (M10), compound (M33) wherein A1 is -NR6- can be produced by subjecting compound (M32) to dehydration condensation according to step (E-3). [Wherein R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, methanol, ethanol, propanol , Alcohols such as butanol and pentanol, and mixtures thereof.
  • an acid or a dehydrating agent can be used as necessary.
  • the acid used in the reaction include sulfonic acids such as p-toluenesulfonic acid, and carboxylic acids such as acetic acid.
  • Examples of the dehydrating agent used in the reaction include phosphorus oxychloride, acetic anhydride, trifluoroacetic anhydride, and the like. Can be mentioned.
  • an acid or a dehydrating agent is usually used at a ratio of 1 mol to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M33) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M33) can be further purified by chromatography, recrystallization and the like.
  • Step (E-3) In compound (M10), compound (M33) in which A1 is —NR6- can be produced by reacting compound (M32) in the presence of a base according to step (E-3). [Wherein R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M33) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M33) can be further purified by chromatography, recrystallization and the like.
  • Step (E-2) Compound (M32) can be produced by reacting compound (M12) and compound (M8) in the presence of a dehydration condensing agent according to step (E-2). [Wherein R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, and BOP reagent.
  • the compound (M8) is usually used in a proportion of 1 to 3 mol, and the dehydrating condensing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 140 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M32) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M32) can be further purified by chromatography, recrystallization and the like.
  • Compound (M32) can be produced by reacting compound (M12) with compound (M34) in the presence of a base.
  • a base wherein R 1, R 2, R 3, R 4, R 5, R 6, A 2 and V 2 represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Aromatic hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof It is done.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M34) is usually used in a proportion of 1 to 3 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M32) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M32) can be further purified by chromatography, recrystallization and the like.
  • Step I15-1 Compound (M36) can be produced by reacting compound (M35) with compound (M20) in the presence of a base. The reaction is usually performed in the presence of a solvent.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, DMF, Examples thereof include acid amides such as NMP, sulfoxides such as DMSO, and mixtures thereof.
  • the base used for the reaction include alkali metal hydrides such as sodium hydride. In the reaction, with respect to 1 mol of the compound (M35), the compound (M20) is usually used in a proportion of 1 to 10 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 150 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (M36) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M36) can be further purified by chromatography, recrystallization and the like.
  • Step I15-2) Compound (M37) can be produced by subjecting compound (M36) to a reduction reaction.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, and halogenated carbonization such as dichloromethane and chloroform.
  • Examples include hydrogens and mixtures thereof.
  • the reducing agent used in the reaction include diisobutylaluminum hydride.
  • the reducing agent is usually used at a ratio of 1 to 2 moles relative to 1 mole of the compound (M36).
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (M37) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M37) can be further purified by chromatography, recrystallization and the like.
  • Examples of the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, nitriles such as acetonitrile, DMF, Examples thereof include acid amides such as NMP, sulfoxides such as DMSO, and mixtures thereof.
  • the base used for the reaction include alkali metal hydrides such as sodium hydride. In the reaction, with respect to 1 mol of the compound (M38), the compound (M20) is usually used in a proportion of 1 to 10 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 150 ° C.
  • the reaction time is usually in the range of 0.5 to 24 hours.
  • the compound (M37) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M37) can be further purified by chromatography, recrystallization and the like.
  • Step I17-1 The reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, alcohols such as methanol and ethanol, water, and a mixture thereof.
  • the base used for the reaction examples include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide.
  • the base is generally used at a ratio of 1 to 10 mol per 1 mol of the compound (M36).
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M39) can be isolated by performing post-treatment operations such as acidification of the reaction mixture, extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. .
  • the isolated compound (M39) can be further purified by chromatography, recrystallization and the like.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include halogenated hydrocarbons such as dichloromethane and chloroform, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used in the reaction include m-chloroperbenzoic acid or hydrogen peroxide water.
  • the reaction can be carried out in the presence of a catalyst as necessary. Examples of the catalyst used for the reaction include sodium tungstate. In the reaction, with respect to 1 mole of the compound (M36), the oxidizing agent is usually used at a ratio of 1 to 5 moles.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite, sodium thiosulfate) or an aqueous solution of a base (for example, sodium bicarbonate) as necessary, dried,
  • a reducing agent for example, sodium sulfite, sodium thiosulfate
  • a base for example, sodium bicarbonate
  • Step I17-3 The reaction is usually performed in the presence of a solvent.
  • a solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, alcohols such as methanol and ethanol, water, and a mixture thereof.
  • the base used for the reaction include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide. In the reaction, the base is usually used at a ratio of 1 to 10 mol per 1 mol of the compound (M40).
  • the reaction temperature of the reaction is usually in the range of 0 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the reaction mixture is acidified, and the compound (M41) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer. .
  • the isolated compound (M41) can be further purified by chromatography, recrystallization, and the like.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include halogenated hydrocarbons such as dichloromethane and chloroform, alcohols such as methanol and ethanol, acetic acid, water, and mixtures thereof.
  • the oxidizing agent used in the reaction include m-chloroperbenzoic acid or hydrogen peroxide water.
  • the reaction can be carried out in the presence of a catalyst as necessary. Examples of the catalyst used for the reaction include sodium tungstate. In the reaction, with respect to 1 mol of the compound (M39), the oxidizing agent is usually used at a ratio of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 120 ° C.
  • the reaction time is usually in the range of 0.1 to 12 hours.
  • the reaction mixture is extracted with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (for example, sodium sulfite, sodium thiosulfate) or an aqueous solution of a base (for example, sodium bicarbonate) as necessary, dried,
  • a reducing agent for example, sodium sulfite, sodium thiosulfate
  • a base for example, sodium bicarbonate
  • compound (M39) in which n is 0 can be produced by subjecting compound (M36) to a hydrolysis reaction in the presence of an acid.
  • the reaction is usually carried out using an aqueous acid solution as a solvent.
  • the acid used for the reaction include mineral acids such as hydrochloric acid, nitric acid, phosphoric acid and sulfuric acid, and carboxylic acids such as acetic acid and trifluoroacetic acid.
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M39) can be isolated by performing post-treatment operations such as extraction of the reaction mixture with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M39) can be further purified by chromatography, recrystallization and the like.
  • Compound (M4) can be produced by chlorinating compound (M2) in the presence of a chlorinating agent.
  • a chlorinating agent e.g., benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether, ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aromatic hydrocarbons such as toluene and xylene, and halogenated carbonization such as dichloromethane and chloroform. Examples include hydrogens and mixtures thereof.
  • Examples of the chlorinating agent used in the reaction include thionyl chloride and oxalyl dichloride.
  • the chlorinating agent is usually used at a ratio of 1 to 5 mol per 1 mol of the compound (M2).
  • the reaction temperature of the reaction is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours. After completion of the reaction, the compound (M4) can be isolated by removing the solvent.
  • the compound (M45) in which A2 is a nitrogen atom can be produced, for example, by the following method.
  • R5 and R6 represent the same meaning as described above, and Xg represents a halogen atom such as a chlorine atom, a bromine atom or an iodine atom.
  • Compound (M43) can be produced by reacting compound (M42) with compound (M46). The reaction is usually performed in the presence or absence of a solvent.
  • Examples of the solvent used in the reaction include water, alcohols such as methanol and ethanol, ethers such as 1,4-dioxane, diethyl ether and THF, esters such as ethyl acetate and butyl acetate, dichloromethane, chloroform and tetrachloride.
  • Examples include carbon, halogenated hydrocarbons such as 1,2-dichloroethane, nitriles such as acetonitrile, aprotic polar solvents such as DMF, NMP, and dimethyl sulfoxide, nitrogen-containing aromatic compounds such as pyridine and quinoline, and mixtures thereof. It is done.
  • This reaction can also be carried out by adding a base as necessary.
  • Examples of the base used in the reaction include nitrogen-containing heterocyclic compounds such as pyridine, picoline, 2,6-lutidine, DBU, 1,5-diazabicyclo [4.3.0] -5-nonene, triethylamine, and N-ethyl. Tertiary amines such as diisopropylamine, and inorganic bases such as potassium carbonate, cesium carbonate, sodium hydroxide and the like.
  • the compound (M46) is usually used at a ratio of 1 to 5 mol per 1 mol of the compound (M42).
  • the reaction temperature of the reaction is usually in the range of 0 to 200 ° C., and the reaction time is usually in the range of 0.1 to 24 hours.
  • reaction mixture After completion of the reaction, the reaction mixture is poured into water and then extracted with an organic solvent, and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture
  • the collected solid can be collected by filtration to isolate compound (M43).
  • the isolated compound (M43) can be further purified by recrystallization, chromatography or the like.
  • Compound (M44) can be produced by reacting compound (M43) with a halogenating agent.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used for the reaction include water, acetic acid, 1,4-dioxane, diethyl ether, THF and other ethers, ethyl acetate, butyl acetate and other esters, dichloromethane, chloroform, carbon tetrachloride, 1,2- Examples thereof include halogenated hydrocarbons such as dichloroethane, nitriles such as acetonitrile, aprotic polar solvents such as DMF and NMP, and mixtures thereof.
  • halogenating agent used in the reaction examples include chlorinating agents such as N-chlorosuccinimide and chlorine, brominating agents such as N-bromosuccinimide and bromine, and chlorinating agents such as N-iodosuccinimide and iodine.
  • the halogenating agent is usually used in a proportion of 1 to 3 mol per 1 mol of the compound (M43).
  • the reaction temperature of the reaction is usually in the range of ⁇ 10 to 100 ° C., and the reaction time is usually in the range of 0.1 to 24 hours.
  • reaction mixture After completion of the reaction, the reaction mixture is poured into water and then extracted with an organic solvent, and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture
  • the collected solid can be collected by filtration to isolate the compound (M44).
  • the isolated compound (M44) can be further purified by recrystallization, chromatography or the like.
  • Compound (M45) can be produced by reacting compound (M44) with an aminating agent in the presence of a copper compound.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include water, alcohols such as methanol and ethanol, ethers such as 1,4-dioxane, diethyl ether and THF, esters such as ethyl acetate and butyl acetate, dichloromethane, chloroform and tetrachloride.
  • Carbon, halogenated hydrocarbons such as 1,2-dichloroethane, nitriles such as acetonitrile, aprotic polar solvents such as DMF, NMP, and dimethyl sulfoxide, nitrogen-containing aromatic compounds such as pyridine and quinoline, and mixtures thereof Can be mentioned.
  • the aminating agent used in the reaction include ammonia, aqueous ammonia, and lithium amide.
  • Examples of the copper compound used in the reaction include copper, copper (I) iodide, copper (I) oxide, copper (II) oxide, acetylacetone copper (II), copper acetate (II), and copper (II) sulfate. It is done.
  • This reaction can also be performed by adding a ligand as necessary.
  • the ligand used in the reaction include acetylacetone, salen, and phenanthroline.
  • This reaction can also be performed by adding a base as necessary.
  • the base used in the reaction include nitrogen-containing heterocyclic compounds such as pyridine, picoline, 2,6-lutidine, DBU, 1,5-diazabicyclo [4.3.0] -5-nonene, triethylamine, and N-ethyl.
  • examples include tertiary amines such as diisopropylamine, and inorganic bases such as tripotassium phosphate, potassium carbonate, cesium carbonate, and sodium hydroxide.
  • the aminating agent is usually used in a proportion of 1 to 5 mol
  • the copper compound is usually used in a proportion of 0.02 to 0.5 mol per 1 mol of the compound (M44).
  • a base is used in a proportion of 1 to 5 mol if necessary.
  • the reaction temperature of the reaction is usually in the range of 30 to 200 ° C.
  • the reaction time is usually in the range of 0.1 to 48 hours.
  • the reaction mixture is poured into water and then extracted with an organic solvent, and the organic layer is concentrated; the reaction mixture is poured into water and the resulting solid is collected by filtration; or formed in the reaction mixture
  • the collected solid can be collected by filtration to isolate compound (M45).
  • the isolated compound (M45) can be further purified by recrystallization, chromatography or the like.
  • Step (A-2) Compound (M22) can be produced by reacting compound (M18) and compound (M2) in the presence of a dehydration condensing agent according to step (A-2). [Wherein, R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above. ] The reaction is usually performed in the presence of a solvent.
  • solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane
  • aliphatic hydrocarbons such as hexane, heptane, and octane
  • aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, and BOP reagent.
  • the compound (M2) is usually used in a proportion of 1 to 3 mol, and the dehydrating condensing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 140 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M22) can be isolated by performing post-treatment operations such as water addition to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M22) can be further purified by chromatography, recrystallization and the like.
  • Step (B-2) Compound (M22) can be produced by reacting compound (M18) and compound (M4) in the presence of a base according to step (B-2).
  • a base a base
  • R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Aromatic hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, and mixtures thereof It is done.
  • Examples of the base used in the reaction include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine. It is done.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol, and the base is usually used in a proportion of 1 to 10 mol.
  • the reaction temperature of the reaction is usually in the range of ⁇ 20 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M22) can be isolated by performing post-treatment operations such as water addition to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M22) can be further purified by chromatography, recrystallization and the like.
  • Step (E-1) Compound (M47) in which A1 is an oxygen atom in compound (M10) can be produced by reacting compound (M15) with compound (M8) according to step (E-1). [Wherein R 1, R 2, R 3, R 4, R 5, A 2, n and V 2 represent the same meaning as described above. ] Compound (M47) can be produced according to the method described in (Production Method 6) using Compound (M8) instead of Compound (M2).
  • Step (E-2) Compound (M48) in which A1 is an oxygen atom in compound (M9) can be produced by reacting compound (M15) with compound (M8) according to step (E-2).
  • compound (M49) in which A1 is a sulfur atom in compound (M9) can be produced by reacting compound (M18) with compound (M8).
  • R1, R2, R3, R4, R5, A2 and V2 represent the same meaning as described above.
  • Compound (M48) can be produced according to the method described in (Intermediate Production Method 6) using Compound (M8) instead of Compound (M2).
  • Compound (M49) can be produced according to the method described in (Intermediate Production Method 21) using Compound (M8) instead of Compound (M2).
  • Step (E-3) Compound (M47) in which A1 is an oxygen atom in compound (M10) can be produced by cyclizing compound (M48) according to step (E-3).
  • compound (M50) in which A1 is a sulfur atom in compound (M10) can be produced by cyclizing compound (M49) according to step (E-3).
  • R1, R2, R3, R4, R5, A2 and V2 represent the same meaning as described above.
  • compound (M48) instead of compound (M17) compound (M47) can be produced according to the method described in (Production Method 8) or (Production Method 9).
  • compound (M49) instead of compound (M22) compound (M50) can be produced according to the method described in (Production Method 21).
  • Step (F-1) Compound (M11) can be produced by reacting compound (M10) with sodium sulfide, sodium hydrogen sulfide or hydrogen sulfide according to step (F-1). [Wherein, R 1, R 2, R 3, R 4, R 5, A 1, A 2 and V 2 represent the same meaning as described above. ] Compound (M11) can be produced according to the method described in (Production Process 16) using sodium sulfide, sodium hydrogen sulfide or hydrogen sulfide instead of compound (M20). When sodium sulfide or sodium hydrogen sulfide is used, it is usually carried out without adding a base.
  • Compound (M7) can be produced by reacting compound (M51) with compound (M2). [Wherein, R1, R2, R3, R4, R5, A2 and n represent the same meaning as described above. ]
  • Compound (M51) can be produced by subjecting compound (M29) to a reduction reaction.
  • the reduction reaction can be performed in the presence of a reducing agent such as iron powder or zinc powder; an acid such as hydrochloric acid or acetic acid; and water.
  • the reaction is usually performed in the presence of a solvent.
  • the solvent used in the reaction examples include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, esters such as ethyl acetate and butyl acetate, alcohols such as methanol and ethanol, Examples thereof include acid amides such as DMF and NMP, and mixtures thereof.
  • the reducing agent is usually used in a proportion of 3 to 10 mol per 1 mol of the compound (M29).
  • the reaction temperature is usually in the range of 0 to 100 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M51) can be isolated by post-treatment such as addition of water to the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer.
  • the isolated compound (M51) can also be purified by chromatography, recrystallization, and the like.
  • the reaction is usually performed in the presence or absence of a solvent.
  • the solvent used in the reaction include ethers such as THF, ethylene glycol dimethyl ether, tert-butyl methyl ether, and 1,4-dioxane, aliphatic hydrocarbons such as hexane, heptane, and octane, and aromatics such as toluene and xylene.
  • Group hydrocarbons such as chlorobenzene, esters such as ethyl acetate and butyl acetate, nitriles such as acetonitrile, acid amides such as DMF and NMP, sulfoxides such as DMSO, pyridine, quinoline and the like
  • Examples thereof include nitrogen-containing aromatic compounds and mixtures thereof.
  • Examples of the dehydrating condensing agent used in the reaction include WSC, carbodiimides such as 1,3-dicyclohexylcarbodiimide, and BOP reagent.
  • the compound (M2) is usually used in a proportion of 1 to 3 mol, and the dehydrating condensing agent is usually used in a proportion of 1 to 5 mol.
  • the reaction temperature of the reaction is usually in the range of 0 to 140 ° C.
  • the reaction time is usually in the range of 0.1 to 24 hours.
  • the compound (M7) can be isolated by performing post-treatment operations such as pouring water into the reaction mixture, extraction with an organic solvent, and drying and concentration of the organic layer. The isolated compound (M7) can be further purified by chromatography, recrystallization and the like.
  • the compound (M4) can replace with a compound (M2) and a compound (M4) can be used, and a compound (M7) can also be manufactured according to the said method.
  • the compound (M4) is usually carried out without adding a dehydrating condensation agent.
  • a base can be added as necessary.
  • the base include alkali metal carbonates such as sodium carbonate and potassium carbonate, tertiary amines such as triethylamine and diisopropylethylamine, and nitrogen-containing aromatic compounds such as pyridine and 4-dimethylaminopyridine.
  • the compound (M4) is usually used in a proportion of 1 to 3 mol
  • the base is usually used in a proportion of 1 to 10 mol.
  • Compound (M1) can be produced by reacting compound (M52) with an aminating agent. [Wherein, Xg, R5, A1 and A2 represent the same meaning as described above. ] Compound (M1) can be produced according to the method described in Step (I20-3) of (Intermediate Production Method 20) using Compound (M52) instead of Compound (M44).
  • R1 to R5, A1, A2, and n represent symbols in the condensed heterocyclic compound represented by the formula (1).
  • the present carboxamide compound is, for example, a compound described in International Publication No. 86/02641 pamphlet and International Publication No. 92/12970 pamphlet, and can be produced by the methods described therein.
  • present carboxamide compound examples include the following.
  • a carboxamide compound represented by the following formula (2a) (hereinafter referred to as the present carboxamide compound (2a));
  • a carboxamide compound represented by the following formula (2b) (hereinafter referred to as the present carboxamide compound (2b));
  • a carboxamide compound represented by the following formula (2c) (hereinafter referred to as the present carboxamide compound (2c));
  • a carboxamide compound represented by the following formula (2d) hereeinafter referred to as the present carboxamide compound (2d)
  • a carboxamide compound represented by the following formula (2e) hereinafter referred to as the present carboxamide compound (2e)).
  • the harmful arthropod control composition of the present invention may be a mixture of the present condensed heterocyclic compound and the present carboxamide compound, but usually the mixed heterocyclic compound, the present carboxamide compound and an inert carrier are mixed. If necessary, add surfactants and other formulation adjuvants, and use those formulated into oils, emulsions, flowables, wettable powders, granular wettable powders, powders, granules, etc. It is done. Moreover, the above-mentioned formulated harmful arthropod control composition can be used as a harmful arthropod control agent as it is or by adding other inactive ingredients.
  • the total amount of the present condensed heterocyclic compound and the present carboxamide compound in the harmful arthropod control composition of the present invention is usually 0.1% to 100% by weight, preferably 0.2 to 90% by weight, more preferably 1%. It is in the range of ⁇ 80 wt%.
  • examples of the inert carrier used for formulation include a solid carrier and a liquid carrier.
  • examples of the solid support include clays (kaolin clay, diatomaceous earth, bentonite, fusami clay, acidic clay), synthetic hydrous silicon oxide, talc, ceramic, and other inorganic minerals (sericite, quartz, sulfur, activated carbon, calcium carbonate).
  • polyester resin such as nylon-6, nylon-11, nylon-66, polyamide resin, polyvinyl chloride, polyvinylidene chloride, vinyl chloride-propylene copolymer).
  • liquid carriers examples include water, alcohols (methanol, ethanol, isopropyl alcohol, butanol, hexanol, benzyl alcohol, ethylene glycol, propylene glycol, phenoxyethanol, etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.), aromatic hydrocarbons.
  • alcohols methanol, ethanol, isopropyl alcohol, butanol, hexanol, benzyl alcohol, ethylene glycol, propylene glycol, phenoxyethanol, etc.
  • ketones acetone, methyl ethyl ketone, cyclohexanone, etc.
  • aromatic hydrocarbons examples include water, alcohols (methanol, ethanol, isopropyl alcohol, butanol, hexanol, benzyl alcohol, ethylene glycol, propylene glycol, phenoxyethanol, etc.
  • ketones acetone, methyl ethyl ket
  • Acid amides N, N-dimethylformamide, N, N-dimethylacetamide, etc.
  • halogenated hydrocarbons diichloromethane, trichloroethane, carbon tetrachloride, etc.
  • sulfoxides dimethylsulfoxide, etc.
  • propylene carbonate and vegetable oil Soybean oil, cottonseed oil, etc.
  • surfactant examples include nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyethylene glycol fatty acid ester, and the like, and alkyl sulfonates, alkyl benzene sulfonates, alkyl sulfates, and the like.
  • nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyethylene glycol fatty acid ester, and the like
  • alkyl sulfonates alkyl benzene sulfonates, alkyl sulfates, and the like.
  • An ionic surfactant is mentioned.
  • formulation adjuvants include fixing agents, dispersants, colorants and stabilizers, such as casein, gelatin, saccharides (starch, gum arabic, cellulose derivatives, alginic acid, etc.), lignin derivatives, bentonite, Synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acids, etc.), PAP (isopropyl acid phosphate), BHT (2,6-di-tert-butyl-4-methylphenol), BHA (2-tert- And a mixture of butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol).
  • fixing agents such as casein, gelatin, saccharides (starch, gum arabic, cellulose derivatives, alginic acid, etc.), lignin derivatives, bentonite, Synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acids, etc.), PAP (iso
  • the content ratio of the present condensed heterocyclic compound and the present carboxamide compound in the harmful arthropod control composition of the present invention is not particularly limited, but the present carboxamide is used with respect to 1000 parts by weight of the present condensed heterocyclic compound.
  • the compound is usually 1 to 1000000 parts by weight, preferably 2 to 10000 parts by weight. That is, the ratio of the content of the present condensed heterocyclic compound and the present carboxamide compound is usually 1000: 1 to 1: 1000, preferably 500: 1 to 1:10 by weight.
  • the harmful arthropod can be controlled by applying an effective amount of the harmful arthropod control composition of the present invention to the plant or the soil where the plant is cultivated.
  • harmful arthropods for which the composition of the present invention is effective include harmful insects and harmful mites. Specific examples of such harmful arthropods include the following.
  • Hemiptera small brown planthopper (Laodelphax striatellus), brown planthopper (Nilaparvata lugens), planthoppers such as Sejirounka (Sogatella furcifera), green rice leafhopper (Nephotettix cincticeps), Taiwan green rice leafhopper (Nephotettix virescens), tea Roh green leafhopper (Empoasca onukii) such as Leafhoppers, cotton aphids (Aphis gossypii), peach aphids (Myzus persicae), radish aphids (Brevicoryne brassicae), aphid spiraecola, tulip beetle aphids Macrosiphum euphorbiae, potato beetle aphids (Aulacorthum solani), wheat beetle aphids (Rhopalosiphum aphids), citrus a
  • Lepidoptera rice stem borer (Chilo suppressalis), Sankameiga (Tryporyza incertulas), leaf roller (Cnaphalocrocis medinalis), Watanomeiga (Notarcha derogata), Indian meal moth (Plodia interpunctella), the European corn borer (Ostrinia furnacalis), high Madara Roh moth (Hellula undalis), Common moths such as Shibatatsuga (Pediasia teterrellus), Lotus moth (Spodoptera litura), Spodoptera exigua, Ayuyoto (Pseudaletia separata), Yotoga Mistra brasicae, Agrotis ipsilon, Tamanaginuawa (Prusia nigrisigna), Trichopulsia, Heliotis, Helicoberpa, etc.
  • Azukiyamamushiga Movsumuraeses azukivivora
  • Apple wolfberry Adoxophyes orana fascita
  • Chanokokumonmonamiki Adoxophyces honmai.
  • Chamonaki Homomona Giant moths of the genus Arsipus fuscocpreaneus, Codling moth (Cydia pomonella), etc.
  • Genus Euplottis, etc. Suga such as Plutella xylostella, Pterinophora gossypiella potato (Pthorimaea operculella), etc .
  • Hitriga and iga Tinea translucens).
  • Thrips of the order Thrips thrips (Franklinella occidentalis), Thrips palmi, etc.
  • Diptera seedcorn maggot (Delia platura), onion maggot (Delia antiqua) Anthomyiidae such as, rice leafminer (Agromyza oryzae), rice Hime leafminer (Hydrellia griseola), tomato leafminer, (Liriomyza sativae), legume leafminer (Liriomyza trifolii) , Leafworms such as Chlamatomyia horticola, leafhoppers such as Chlorops oryzae, Dacucus cucurbitae, and Ceramitobaceae.
  • Anthomyiidae such as, rice leafminer (Agromyza oryzae), rice Hime leafminer (Hydrellia griseola), tomato leafminer, (Liriomyza sativae), legume leafminer (Liriomyza trifolii) ,
  • Leafworms such as Chlamatomyia horticola, leafhopper
  • Coleoptera pests Western Corn Rootworm (Diabrotica virgifera virgifera), corn rootworm such as southern corn rootworm (Diabrotica undecimpunctata howardi), cupreous chafer (Anomala cuprea), rufocuprea (Anomala rufocuprea), chafers such as Japanese beetle (Popillia japonica) , Weeweevil (Sitophilus zeamais), Rice weevil (Lissohopoptrus oryzophilus), Rice weevil (Echinocnemus squameus), Cotton weevil (Anthonomus grandis), Shiba souzo s venatus) weevil such as, Chai loco Meno mealworm (Tenebrio molitor), mealworm such as red flour beetle (Tribolium castaneum), Inedorooimushi (Oulema oryzae), cucurbit leaf beetle (Aulacophora
  • the application amount is usually 1 to 10,000 g in terms of the amount of the present condensed heterocyclic compound per 10,000 m 2.
  • the harmful arthropod control agent of the present invention is formulated into an emulsion, a wettable powder, a flowable agent, etc., it is usually applied by diluting with water so that the active ingredient concentration becomes 0.01 to 10,000 ppm. Granules, powders and the like are usually applied as they are.
  • These preparations and water dilutions of these preparations may be sprayed directly on harmful arthropods or plants such as crops to be protected from harmful arthropods, and harmful arthropods that inhabit the soil of cultivated land. You may treat to this soil in order to control.
  • the harmful arthropod control agent of the present invention can be used in farmland where the following “crop” is cultivated.
  • Agricultural crops corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, peanut, buckwheat, sugar beet, rapeseed, sunflower, sugarcane, tobacco, etc.
  • Vegetables Solanum vegetables (eggplants, tomatoes, peppers, peppers, potatoes, etc.), Cucurbitaceae vegetables (cucumbers, pumpkins, zucchini, watermelons, melons, etc.), cruciferous vegetables (radish, turnip, horseradish, kohlrabi, Chinese cabbage, cabbage) , Mustard, broccoli, cauliflower, etc.), asteraceae vegetables (burdock, shungiku, artichoke, lettuce, etc.), liliaceae vegetables (leek, onion, garlic, asparagus), celeryaceae vegetables (carrot, parsley, celery, American scallop, etc.) ), Red crustacean vegetables (spinach, chard, etc.); Fruit trees: apples, pears, Japanese pears, quince, quince, etc., nuclear fruits (peaches, plums, nectarines, ume, sweet cherry, apricots, prunes, etc.), citrus (citrus mandarin, orange, lemon, lime, grapefruit) ), Nuts (
  • Trees other than fruit trees tea, mulberry, flowering trees (Satsuki, camellia, hydrangea, sasanqua, shikimi, sakura, yurinoki, crape myrtle, snapdragon, etc.), roadside trees (ash, birch, dogwood, eucalyptus, ginkgo, lilac, maple, oak) , Poplar, redwood, fu, sycamore, zelkova, blackfish, Japanese amberjack, eel, pine, pine, spruce, yew, elm, Japanese cypress, etc.), coral jug, dogwood, cedar, cypress, croton, masaki, kanamochi, etc.
  • Lawn Shiba (Nasis, Pleurotus, etc.), Bermudagrass (Neurodonidae, etc.), Bentgrass (Oleoptera, Hykonukagusa, Odonoptera, etc.), Bluegrass (Nagahagusa, Oosuzunokatabira, etc.), Fescue (Oonishi nokegusa, Drosophila, etc.) , Grass, etc.), ryegrass (rat, wheat, etc.), anemonefish, blue whale, etc.
  • Crop includes genetically modified crops.
  • Production Example 1 A mixture of 1.0 g of N2-methyl-5-trifluoromethylpyridine-2,3-diamine, 0.96 g of 2-ethylsulfanylbenzaldehyde, 1.80 g of sodium hydrogensulfite and 10 ml of DMF was heated and stirred at 160 ° C. for 5 hours. The reaction mixture was ice-cooled, water was added, and the precipitated crystals were collected by filtration, and washed with water and then hexane.
  • This condensed heterocyclic compound 8 1H-NMR (CDCl3) ⁇ : 8.73 (1H, d), 8.28 (1H, d), 8.22 (1H, dd), 7.83 (1H, td), 7.69 (1H, td), 7.50 (1H, dd), 4.60-4.48 (1H, m), 3.38-3.26 (1H, m), 3.05-2.95 (1H, m) , 1.77-1.71 (6H, m), 1.27 (3H, t)
  • This condensed heterocyclic compound 9 1H-NMR (CDCl3) ⁇ : 8.71 (1H, d), 8.24-8.22 (2H, m), 7.85-7.78 (2H, m), 7.55-7.52 (1H, m), 4.33-4.26 (1H, m), 3.72-3.62 (1H, m), 3.44-3.34 (1H, m), 1.77-1 .69 (6H, m), 1.28 (3H, t)
  • the present condensed heterocyclic compound 10 1H-NMR (CDCl3) ⁇ : 8.74 (1H, s), 8.31 (1H, s), 7.53-7.47 (3H, m), 7.39-7.31 (1H, m ), 3.55-3.49 (1H, m), 2.90 (2H, q), 1.25 (3H, t), 1.01-0.94 (2H, m), 0.93- 0.86 (2H, m)
  • This condensed heterocyclic compound 11 1H-NMR (CDCl3) ⁇ : 8.77 (1H, d), 8.29-8.26 (2H, m), 7.85-7.79 (2H, m), 7.72-7.67 (1H, m), 3.57-3.51 (1H, m), 3.49-3.39 (1H, m), 3.09-2.95 (1H, m), 1.34 (3H , T), 1.29-1.16 (1H, m), 1.09-0.92 (2H, m), 0.80-0.65 (1H, m)
  • This condensed heterocyclic compound 12 1H-NMR (CDCl3) ⁇ : 8.76 (1H, s), 8.27-8.22 (2H, m), 7.87-7.78 (2H, m), 7.65 (1H, dd) ), 3.60 (2H, brs), 3.39-3.33 (1H, m), 1.29 (3H, t), 1.11-1.11 (2H, m), 0.93 ( 2H, brs).
  • the present condensed heterocyclic compound 14 1H-NMR (CDCl3) ⁇ : 8.62 (1H, s), 8.26-8.23 (2H, m), 7.83 (1H, td), 7.70 (1H, td), 7. 62 (1H, dd), 6.90 (1H, t), 3.89 (3H, s), 3.42-3.32 (1H, m), 3.02-2.92 (1H, m) , 1.30 (3H, t)
  • This condensed heterocyclic compound 15 1H-NMR (CDCl3) ⁇ : 8.61 (1H, s), 8.24-8.19 (2H, m), 7.87-7.78 (2H, m), 7.58 (1H, dd) ), 6.89 (1H, t), 3.71 (3H, s), 3.43 (2H, q), 1.25 (3H, t)
  • Production Example 17 A mixture of 1.64 g of 2-ethylsulfanyl-N- (2-methylamino-5-trifluoromethylphenyl) -benzamide, 1.76 g of p-toluenesulfonic acid monohydrate and 50 ml of xylene at 150 ° C. for 1 hour, Stir with heating to reflux. To the reaction mixture cooled to room temperature, a saturated aqueous sodium hydrogen carbonate solution was poured, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium bicarbonate solution and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure.
  • the obtained residue was subjected to silica gel column chromatography to give 2- (2-ethylsulfanylphenyl) -1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter referred to as the present condensed heterocyclic compound 17). 1.40 g was obtained.
  • the present condensed heterocyclic compound 17 1H-NMR (CDCl3) ⁇ : 8.12-8.10 (1H, m), 7.61-7.58 (1H, m), 7.53-7.44 (4H, m), 7.38 ⁇ 7.32 (1H, m), 3.69 (3H, s), 2.84 (2H, q), 1.22 (3H, t)
  • the present condensed heterocyclic compound 18 1H-NMR (CDCl3) ⁇ : 8.24-8.20 (1H, m), 8.10-8.07 (1H, m), 7.83-7.78 (1H, m), 7.70 -7.62 (2H, m), 7.57-7.51 (2H, m), 3.79 (3H, s), 3.36-3.26 (1H, m), 2.98-2 .88 (1H, m), 1.26 (3H, t)
  • the obtained residue was subjected to silica gel column chromatography to obtain 0.98 g of 2- (2-ethylsulfanylphenyl) -5-trifluoromethylbenzoxazole (hereinafter referred to as the present condensed heterocyclic compound 20).
  • the present condensed heterocyclic compound 20 1H-NMR (CDCl3) ⁇ : 8.19-8.15 (2H, m), 7.71-7.67 (1H, m), 7.66-7.63 (1H, m), 7.52 -7.47 (1H, m), 7.45-7.42 (1H, m), 7.31-7.27 (1H, m), 3.06 (2H, q), 1.44 (3H , T)
  • the present condensed heterocyclic compound 23 0.53 g of [5,4-b] pyridine (hereinafter referred to as the present condensed heterocyclic compound 23) was obtained.
  • the present condensed heterocyclic compound 23 1H-NMR (CDCl3) ⁇ : 8.67 (1H, s), 8.40 (1H, s), 8.25 (1H, d), 7.53 (1H, t), 7.45 (1H, d), 7.32 (1H, t), 3.08 (2H, q), 1.45 (3H, t)
  • the present condensed heterocyclic compound 24 1H-NMR (CDCl3) ⁇ : 8.73-8.72 (1H, m), 8.41-8.38 (2H, m), 8.36-8.33 (1H, m), 7.90 -7.84 (1H, m), 7.74-7.69 (1H, m), 3.45-3.35 (1H, m), 3.00-2.90 (1H, m), 1 .40 (3H, t)
  • the obtained residue was subjected to silica gel column chromatography to obtain 0.50 g of 2- (2-ethylsulfanylphenyl) -5-trifluoromethylbenzothiazole (hereinafter referred to as the present condensed heterocyclic compound 26).
  • the present condensed heterocyclic compound 26 1H-NMR (CDCl3) ⁇ : 8.41-8.39 (1H, m), 8.06-8.00 (2H, m), 7.66-7.62 (1H, m), 7.55 -7.51 (1H, m), 7.48-7.42 (1H, m), 7.37-7.32 (1H, m), 2.96 (2H, q), 1.33 (3H , T)
  • the present condensed heterocyclic compound 28 1H-NMR (CDCl3) ⁇ : 8.33-8.31 (1H, m), 8.26-8.23 (1H, m), 8.10-8.06 (1H, m), 7.81 -7.69 (4H, m), 3.75 (2H, q), 1.36 (3H, t)
  • This condensed heterocyclic compound 29 1H-NMR (CDCl3) ⁇ : 8.70 (1H, d), 8.29 (1H, d), 8.27 (1H, d), 7.84 (1H, t), 7.71 (1H, t), 7.60 (1H, d), 3.90 (3H, s), 3.43-3.33 (1H, m), 3.04-2.94 (1H, m), 1.31 (3H, t)
  • This condensed heterocyclic compound 31 1.05 g was obtained.
  • This condensed heterocyclic compound 31 1H-NMR (CDCl3) ⁇ : 8.70-8.68 (1H, m), 8.31-8.28 (1H, m), 7.43-7.38 (1H, m), 7.17 -7.13 (1H, m), 7.04-6.98 (1H, m), 3.75 (3H, s), 2.89 (2H, q), 1.26 (3H, t)
  • the present condensed heterocyclic compound 32 1H-NMR (CDCl3) ⁇ : 8.76-8.75 (1H, m), 8.31-8.30 (1H, m), 8.01-7.98 (1H, m), 7.65 -7.61 (1H, m), 7.41-7.36 (1H, m), 3.90 (3H, s), 3.47-3.37 (1H, m), 3.04-2 .94 (1H, m), 1.33 (3H, t)
  • This condensed heterocyclic compound 33 1H-NMR (CDCl3) ⁇ : 8.76-8.74 (1H, m), 8.29-8.27 (1H, m), 7.97-7.94 (1H, m), 7.60 -7.51 (2H, m), 3.72 (3H, s), 3.44 (2H, q), 1.28 (3H, t)
  • the obtained residue was subjected to silica gel column chromatography to give 2- (2-ethylsulfanyl-4-trifluoromethylphenyl) -3-methyl-6-trifluoromethyl-3H-imidazo [4,5-b] pyridine.
  • the present condensed heterocyclic compound 34 1.10 g was obtained.
  • the present condensed heterocyclic compound 34 1H-NMR (CDCl3) ⁇ : 8.75-8.73 (1H, m), 8.35-8.33 (1H, m), 7.70-7.68 (1H, m), 7.62 -7.56 (2H, m), 3.79 (3H, s), 2.95 (2H, q), 1.28 (3H, t)
  • the present condensed heterocyclic compound 36 1H-NMR (CDCl3) ⁇ : 8.68 (1H, d), 8.29-8.24 (2H, m), 7.87-7.81 (1H, m), 7.74-7.68 (1H, m), 7.61 (1H, dd), 3.91 (3H, s), 3.43-3.32 (1H, m), 3.05-2.94 (1H, m), 1.31 (3H, t)
  • the present condensed heterocyclic compound 37 1H-NMR (CDCl3) ⁇ : 8.67 (1H, d), 8.26-8.22 (2H, m), 7.87-7.81 (2H, m), 7.59-7.55 (1H, m), 3.73 (3H, s), 3.43 (2H, q), 1.26 (3H, t).
  • Trifluoromethylphenyl) -3-methyl-6-trifluoromethyl-3H-imidazo [4,5-b] pyridine (hereinafter referred to as the present condensed heterocyclic compound 38) 0.51 g
  • 2- (2- Ethylsulfonyl-4-trifluoromethylphenyl) -3-methyl-6-trifluoromethyl-3H-imidazo [4,5-b] pyridine (hereinafter referred to as this condensed heterocyclic compound) 39 and referred to.) was obtained 0.26g.
  • the present condensed heterocyclic compound 38 1H-NMR (CDCl3) ⁇ : 8.79-8.78 (1H, m), 8.57-8.55 (1H, m), 8.35-8.34 (1H, m), 7.97 -7.94 (1H, m), 7.77 (1H, d), 3.94 (3H, s), 3.53-3.43 (1H, m), 3.07-2.98 (1H) , M), 1.36 (3H, t)
  • the present condensed heterocyclic compound 39 1H-NMR (CDCl3) ⁇ : 8.78-8.76 (1H, m), 8.51-8.49 (1H, m), 8.31-8.30 (1H, m), 8.12 -8.09 (1H, m), 7.74 (1H, d), 3.74 (3H, s), 3.48 (2H, q), 1.29 (3H, t)
  • Production Example 40 A mixture of 0.56 g of 3-amino-5- (trifluoromethyl) pyridine-2-thiol, 0.52 g of 2-ethylsulfanylbenzoic acid, 0.80 g of WSC, 39 mg of HOBt and 6 ml of pyridine was stirred at 60 ° C. for 2 hours. Water was poured into the reaction mixture allowed to cool, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure.
  • the present condensed heterocyclic compound 41 1H-NMR (CDCl3) ⁇ : 8.90 (1H, d), 8.49 (1H, d), 8.37 (1H, dd), 7.99 (1H, dd), 7.81 (1H, td), 7.67 (1H, td), 3.52-3.42 (1H, m), 3.01-2.92 (1H, m), 1.45 (3H, t).
  • the present condensed heterocyclic compound 42 1H-NMR (CDCl3) ⁇ : 8.92 (1H, d), 8.52 (1H, d), 8.25 (1H, dd), 7.84-7.71 (3H, m), 3. 73 (2H, q), 1.37 (3H, t).
  • Methylsulfanyl-3-methyl-3H-imidazo [4,5-b] pyridine (hereinafter referred to as the present condensed heterocyclic compound 43) and 2- (2-ethylsulfinyl-phenyl) -6-trifluoromethylsulfanyl- 3-methyl-3H-imidazo [4,5-b] pyridine (hereinafter referred to as the present condensed heterocyclic compound 44) was obtained.
  • the present condensed heterocyclic compound 43 1H-NMR (CDCl3) ⁇ : 8.68 (1H, d), 8.36 (1H, d), 8.21 (1H, dd), 7.87-7.77 (2H, m), 7.
  • This condensed heterocyclic compound 45 1H-NMR (CDCl3) ⁇ : 8.77 (1H, d), 8.55 (1H, d), 8.24 (1H, dd), 7.90-7.83 (2H, m), 7. 61 (1H, dd), 3.75 (3H, s), 3.43 (2H, q), 1.26 (3H, t)
  • the present condensed heterocyclic compound 46 1H-NMR (CDCl3) ⁇ : 9.05 (1H, d), 8.65 (1H, d), 8.26-8.23 (1H, m), 7.90-7.85 (2H, m ), 7.61-7.57 (1H, m), 3.77 (3H, s), 3.41 (2H, q), 1.27 (3H, t)
  • the obtained residue was subjected to silica gel column chromatography to give 2- [2-ethylsulfanyl-4- (trifluoromethyl) phenyl] -6- (trifluoromethyl) thiazolo [5,4-b] pyridine (hereinafter, This is referred to as the present condensed heterocyclic compound 47.) 0.11 g was obtained.
  • the present condensed heterocyclic compound 47 1H-NMR (CDCl3) ⁇ : 8.90 (1H, d), 8.61 (1H, d), 8.14 (1H, d), 7.75 (1H, s), 7.58 (1H, d), 3.04 (2H, q), 1.38 (3H, t).
  • the obtained residue was subjected to silica gel column chromatography, and 2- [2-ethylsulfonyl 4- (trifluoromethyl) phenyl] -6- (trifluoromethyl) thiazolo [5,4-b] pyridine (hereinafter referred to as the present).
  • This is referred to as a condensed heterocyclic compound 48.
  • 0.11 g was obtained.
  • the present condensed heterocyclic compound 48 1H-NMR (CDCl3) ⁇ : 8.95 (1H, s), 8.55 (1H, s), 8.52 (1H, s), 8.07 (1H, d), 7.88 (1H, d), 3.77 (2H, q), 1.40 (3H, t).
  • the present condensed heterocyclic compound 52 1H-NMR (CDCl3) ⁇ : 8.71-8.70 (1H, m), 8.50-8.49 (1H, m), 8.38-8.36 (1H, m), 8.12 -8.08 (1H, m), 7.74-7.71 (1H, m), 3.72 (3H, s), 3.49 (2H, q), 1.29 (3H, t).
  • the present condensed heterocyclic compound 53 1H-NMR (CDCl3) ⁇ : 9.08-9.07 (1H, m), 8.68-8.66 (1H, m), 8.52-8.50 (1H, m), 8.16 -8.12 (1H, m), 7.76-7.73 (1H, m), 3.78 (3H, s), 3.46 (2H, q), 1.30 (3H, t)
  • the obtained residue was dissolved in a mixed solution of 7.5 mL of DMF and 30 mL of toluene, and 837 mg of p-toluenesulfonic acid was added at room temperature. The mixture was heated and stirred at 130 ° C. for 8 hours, and then allowed to cool to room temperature. Saturated aqueous sodium hydrogen carbonate solution was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography. This is referred to as the present condensed heterocyclic compound 54.) 97 mg was obtained.
  • the present condensed heterocyclic compound 54 1H-NMR (CDCl3) ⁇ : 12.08-11.87 (1H, m), 8.31 (1H, s), 8.12-7.44 (4H, m), 7.42-7.30 (2H, m), 2.86 (2H, q), 1.22 (3H, t).
  • the present condensed heterocyclic compound 55 1H-NMR (CDCl3) ⁇ : 8.73-8.71 (1H, m), 8.33-8.32 (1H, m), 7.59 (1H, d), 7.50-7.47 (1H, m), 7.30 (1H, d), 3.77 (3H, s), 2.91 (2H, q), 1.27 (3H, t).
  • the present condensed heterocyclic compound 56 1H-NMR (CDCl3) ⁇ : 8.77-8.75 (1H, m), 8.39 (1H, d), 8.32-8.31 (1H, m), 7.84-7.81 (1H, m), 7.49 (1H, d), 3.91 (3H, s), 3.50-3.40 (1H, m), 3.06-2.96 (1H, m), 1.35 (3H, t).
  • the present condensed heterocyclic compound 57 1H-NMR (CDCl3) ⁇ : 8.77-8.75 (1H, m), 8.37 (1H, d), 8.31-8.29 (1H, m), 7.9-7.96. (1H, m), 7.44 (1H, d), 3.72 (3H, s), 3.44 (2H, q), 1.28 (3H, t).
  • the present condensed heterocyclic compound 58 1H-NMR (CDCl3) ⁇ : 8.77-8.74 (1H, m), 8.38-8.36 (1H, m), 8.30-8.27 (1H, m), 8.00 -7.95 (1H, m), 7.63-7.55 (1H, m), 7.43 (1H, d), 7.41-7.30 (2H, m), 3.72 (3H , S), 3.44 (2H, q), 1.28 (3H, t).
  • the residue was subjected to silica gel column chromatography, and 2- (2-ethylsulfonyl-4-trifluoromethyl-phenyl) -6-trifluoromethyl-3H-imidazo [4,5-b] pyridine (hereinafter referred to as the present condensed complex). 9.1 g was obtained.
  • the present condensed heterocyclic compound 60 1H-NMR (DMSO-D6) ⁇ : 14.15 (1H, brs), 8.83 (1H, s), 8.58 (1H, s), 8.41 (1H, d), 8.37 ( 1H, s), 8.19 (1H, d), 3.97 (2H, q), 1.23 (3H, t).
  • the residue was subjected to silica gel column chromatography, and the resulting crystals were washed with hexane to give 2- (2-ethylsulfonyl-phenyl) -6-trifluoromethyl-3H-imidazo [4,5-b] pyridine.
  • the present condensed heterocyclic compound 62 2.5 g was obtained.
  • the present condensed heterocyclic compound 62 1H-NMR (CDCl3) ⁇ : 8.63 (1H, s), 8.35 (1H, s), 8.24 (1H, d), 8.09 (1H, d), 7.83 (1H, t), 7.76 (1H, t), 3.33 (2H, q), 0.88 (3H, t).
  • the present condensed heterocyclic compound 63 0.47 g, 2- (2-ethanesulfonyl-4-trifluoromethoxyphenyl) -3-methyl-6-trifluoromethyl-3H-imidazo [4,5 -B] 0.14 g of pyridine (hereinafter referred to as the present condensed heterocyclic compound 64) was obtained.
  • the present condensed heterocyclic compound 64 1H-NMR (CDCl3) ⁇ : 8.77-8.75 (1H, m), 8.30-8.28 (1H, m), 8.09-8.07 (1H, m), 7.70 ⁇ 7.66 (1H, m), 7.63 (1H, d), 3.74 (3H, s), 3.46 (2H, q), 1.28 (3H, t).
  • Production Example 66-1 A mixture of 0.50 g of 2-amino-4-trifluoromethylphenol, 0.71 g of 2-ethylsulfanyl-4-trifluoromethylbenzoic acid, 0.65 g of WSC and 6 ml of chloroform was stirred at room temperature for 3.5 hours. Saturated aqueous ammonium chloride solution was poured into the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure.
  • the obtained residue was subjected to silica gel column chromatography to give 2- (2-ethylsulfonyl-4-trifluoromethylphenyl) -5-trifluoromethylbenzoxazole (hereinafter referred to as the present condensed heterocyclic compound 130). .34 g was obtained.
  • the present condensed heterocyclic compound 130 1 H-NMR (CDCl 3 ) ⁇ : 8.54 (1H, s), 8.18-8.12 (2H, m), 8.08 (1H, dd), 7.77-7.74 (2H M), 3.90 (2H, q), 1.44 (3H, t).
  • the present condensed heterocyclic compound 66 1H-NMR (CDCl3) ⁇ : 8.51 (1H, s), 8.22 (1H, s), 7.55-7.50 (2H, m), 7.47-7.43 (1H, m ), 7.38-7.32 (1H, m), 5.81 (1H, dq), 3.76 (3H, s), 2.88 (2H, q), 1.24 (3H, t) .
  • This condensed heterocyclic compound 68 1H-NMR (CDCl3) ⁇ : 8.53 (1H, s), 8.26-8.16 (2H, m), 7.88-7.78 (2H, m), 7.59-7.53 (1H, m), 5.82 (1H, dq), 3.70 (3H, s), 3.44 (2H, q), 1.26 (3H, t).
  • This condensed heterocyclic compound 69 1H-NMR (CDCl3) ⁇ : 8.68 (1H, d), 8.29 (1H, d), 7.74-7.68 (1H, m), 7.49-7.40 (2H, m ), 3.73 (3H, s), 2.74 (2H, q), 1.06 (3H, t).
  • the present condensed heterocyclic compound 70 1H-NMR (CDCl3) ⁇ : 8.64 (1H, s), 8.24 (1H, s), 7.65 (1H, d), 7.58 (1H, t), 7.39 (1H, d), 3.72 (3H, s), 3.63-3.47 (1H, m), 3.37-3.22 (1H, m), 1.38-1.30 (3H, m) .
  • the present condensed heterocyclic compound 72 1H-NMR (CDCl3) ⁇ : 8.78-8.76 (1H, m), 8.33-8.31 (1H, m), 8.20 (1H, d), 7.81-7.78 (1H, m), 7.60 (1H, d), 3.93 (3H, s), 3.42-3.32 (1H, m), 3.02-2.92 (1H, m), 1.31 (3H, t).
  • the present condensed heterocyclic compound 76 1H-NMR (CDCl3) ⁇ : 8.73-8.72 (1H, m), 8.28-8.26 (1H, m), 7.84-7.78 (1H, m), 7.55 -7.49 (1H, m), 7.38-7.35 (1H, m), 3.77 (3H, s), 3.50-3.34 (2H, m), 1.34 (3H , T).
  • the present condensed heterocyclic compound 78 1H-NMR (CDCl3) ⁇ : 8.79-8.76 (1H, m), 8.35-8.32 (1H, m), 8.03 (1H, d), 7.87-7.80 (1H, m), 7.43 (1H, t), 3.84 (3H, d), 3.51-3.40 (1H, m), 3.13-3.02 (1H, m), 1.33 (3H, t).
  • This condensed heterocyclic compound 80 1H-NMR (CDCl3) ⁇ : 8.71-8.69 (1H, m), 8.31-8.30 (1H, m), 7.35-7.31 (2H, m), 7.19 -7.15 (1H, m), 3.76 (3H, s), 2.85 (2H, q), 2.46 (3H, s), 1.22 (3H, t).
  • This condensed heterocyclic compound 85 1H-NMR (CDCl3) ⁇ : 8.78-8.76 (1H, m), 8.47-8.46 (1H, m), 8.31-8.30 (1H, m), 8.10 -8.07 (1H, m), 7.76 (1H, d), 3.76 (3H, s), 3.48 (2H, q), 1.28 (3H, t).
  • the present condensed heterocyclic compound 86 1H-NMR (CDCl3) ⁇ : 8.51 (1H, d), 8.19 (1H, d), 7.53-7.42 (3H, m), 7.38-7.29 (1H, m ), 3.73 (3H, s), 2.97-2.83 (4H, m), 1.33-1.19 (6H, m).
  • the present condensed heterocyclic compound 87 1H-NMR (CDCl3) ⁇ : 8.96 (1H, d), 8.54 (1H, d), 8.28-8.18 (1H, m), 7.91-7.80 (2H, m ), 7.63-7.55 (1H, m), 3.74 (3H, s), 3.43 (2H, q), 3.24 (2H, q), 1.38 (3H, t) , 1.26 (3H, t).
  • the present condensed heterocyclic compound 91 1H-NMR (CDCl3) ⁇ : 8.93 (1H, d), 8.52 (1H, d), 8.25 (1H, d), 7.78 (1H, dd), 7.67 (1H, d), 3.76 (2H, q), 1.40 (3H, t).
  • This condensed heterocyclic compound 92 1H-NMR (CDCl3) ⁇ : 8.89 (1H, d), 8.56 (1H, d), 7.56-7.42 (3H, m), 7.39-7.33 (1H, m ), 3.77 (3H, s), 2.89 (2H, q), 1.25 (3H, t).
  • This condensed heterocyclic compound 93 1H-NMR (CDCl3) ⁇ : 8.93 (1H, d), 8.53 (1H, d), 8.26 (1H, dd), 7.84 (1H, td), 7.71 (1H, td), 7.60 (1H, dd), 3.89 (3H, s), 3.42-3.32 (1H, m), 3.05-2.96 (1H, m), 1.31 (3H, t).
  • This condensed heterocyclic compound 94 1H-NMR (CDCl3) ⁇ : 8.91 (1H, d), 8.50 (1H, d), 8.23 (1H, dd), 7.87-7.80 (2H, m), 7.
  • the present condensed heterocyclic compound 96 1H-NMR (CDCl3) ⁇ : 8.09 (1H, s), 7.59-7.42 (5H, m), 7.37-7.31 (1H, m), 3.69 (3H, s) ), 2.85 (2H, q), 1.23 (3H, t).
  • This condensed heterocyclic compound 97 1H-NMR (CDCl3) ⁇ : 8.22 (1H, d), 8.07 (1H, s), 7.80 (1H, t), 7.67 (1H, t), 7.62-7. 52 (3H, m), 3.79 (3H, s), 3.37-3.26 (1H, m), 3.01-2.89 (1H, m), 1.27 (3H, t) .
  • the present condensed heterocyclic compound 100 1H-NMR (CDCl3) ⁇ : 8.69-8.68 (1H, m), 8.28-8.26 (1H, m), 8.07-8.05 (1H, m), 7.50 -7.48 (2H, m), 3.89 (3H, s), 3.44-3.33 (1H, m), 3.01-2.92 (1H, m), 2.58 (3H , S), 1.32 (3H, t).
  • the present condensed heterocyclic compound 102 1H-NMR (CDCl3) ⁇ : 8.81 (1H, d), 8.55 (1H, d), 8.07-8.00 (1H, m), 7.59-7.53 (1H, m ), 7.52-7.45 (1H, m), 7.41-7.33 (1H, m), 2.99 (2H, q), 1.35 (3H, t).
  • This condensed heterocyclic compound 103 1H-NMR (CDCl3) ⁇ : 8.85 (1H, d), 8.59 (1H, d), 8.15 (1H, d), 7.75 (1H, s), 7.59 (1H, d), 3.05 (2H, q), 1.38 (3H, t).
  • the condensed heterocyclic compound 104 1H-NMR (CDCl3) ⁇ : 8.87 (1H, d), 8.50 (1H, d), 8.28-8.22 (1H, m), 7.85-7.76 (2H, m ), 7.74-7.70 (1H, m), 3.74 (2H, q), 1.37 (3H, t).
  • This condensed heterocyclic compound 105 1H-NMR (CDCl3) ⁇ : 8.90 (1H, s), 8.57-8.49 (2H, m), 8.07 (1H, d), 7.88 (1H, d), 3. 77 (2H, q), 1.40 (3H, t).
  • This condensed heterocyclic compound 106 1H-NMR (CDCl3) ⁇ : 8.93 (1H, d), 8.61 (1H, d), 7.45-7.34 (3H, m), 2.91 (2H, q), 1. 27 (3H, t).
  • the present condensed heterocyclic compound 107 1H-NMR (CDCl3) ⁇ : 8.95 (1H, d), 8.55 (1H, d), 8.14 (1H, dd), 7.86 (1H, dd), 7.73 (1H, t), 3.40 (2H, q), 1.28 (3H, t).
  • the present condensed heterocyclic compound 108 1H-NMR (CDCl3) ⁇ : 8.74-8.72 (1H, m), 8.28-8.26 (1H, m), 8.05-8.03 (1H, m), 7.67 ⁇ 7.64 (1H, m), 7.46 (1H, d), 3.71 (3H, s), 3.41 (2H, q), 2.88 (2H, q), 1.37 ( 3H, t), 1.26 (3H, t).
  • the present condensed heterocyclic compound 109 1H-NMR (CDCl3) ⁇ : 8.78-8.76 (1H, m), 8.46-8.44 (1H, m), 8.31-8.30 (1H, m), 8.09 -8.05 (1H, m), 7.76 (1H, d), 3.75 (3H, s), 3.48 (2H, q), 1.27 (3H, t).
  • the present condensed heterocyclic compound 110 1H-NMR (CDCl3) ⁇ : 8.69 (1H, s), 8.33 (1H, s), 8.25 (1H, dd), 8.21 (1H, dd), 7.73-7.
  • the present condensed heterocyclic compound 116 1H-NMR (CDCl3) ⁇ : 8.74-8.72 (1H, m), 8.28-8.25 (1H, m), 8.07-8.05 (1H, m), 7.69 -7.66 (1H, m), 7.47 (1H, d), 3.72 (3H, s), 3.41 (2H, q), 3.18-3.10 (1H, m), 1.37 (6H, d), 1.26 (3H, t).
  • the present condensed heterocyclic compound 120 1H-NMR (CDCl3) ⁇ : 8.71-8.69 (1H, m), 8.27-8.26 (1H, m), 8.09-8.07 (1H, m), 7.70 ⁇ 7.66 (1H, m), 7.62 (1H, d), 3.74 (3H, s), 3.47 (2H, q), 1.28 (3H, t).
  • This condensed heterocyclic compound 121 1H-NMR (CDCl3) ⁇ : 8.11 (1H, s), 7.67 (1H, s), 7.61-7.56 (3H, m), 7.53 (1H, d), 3. 70 (3H, s), 2.93 (2H, q), 1.28 (3H, t).
  • the present condensed heterocyclic compound 122 1H-NMR (CDCl3) ⁇ : 8.53 (1H, d), 8.09 (1H, s), 7.93 (1H, dd), 7.74 (1H, d), 7.64 (1H, d), 7.59 (1H, d), 3.85 (3H, s), 3.51-3.40 (1H, m), 3.06-2.97 (1H, m), 1.32 (3H, t).
  • This condensed heterocyclic compound 128 1 H-NMR (CDCl 3 ) ⁇ : 8.53 (1H, s), 8.19-8.13 (2H, m), 8.07 (1H, dd), 7.77 (1H, dd), 7.69 (1H, d), 3.91 (2H, q), 1.44 (3H, t).
  • Formulation Example 1 5 parts of one of the condensed heterocyclic compounds 1-131, 10 parts of the carboxamide compound (2a), 35 parts of a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1: 1), and Each preparation is obtained by mixing water to make a total amount of 100 parts and finely pulverizing with a wet pulverization method.
  • Formulation Example 2 Of the condensed heterocyclic compounds 1-131, 5 parts, 5 parts of the carboxamide compound (2e), 35 parts of a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1: 1), and Each preparation is obtained by mixing water to make the total amount 100 parts and finely pulverizing with a wet pulverization method.
  • Formulation Example 3 10 parts of the present condensed heterocyclic compounds 1-131, 0.1 part of the present carboxamide compound (2a), a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1: 1) 35 Each formulation is obtained by mixing parts and water to make the total amount 100 parts, and finely pulverizing with a wet pulverization method.
  • Formulation Example 4 10 parts of the present condensed heterocyclic compounds 1-131, 0.1 part of the present carboxamide compound (2e), a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1: 1) 35 Each formulation is obtained by mixing parts and water to make the total amount 100 parts, and finely pulverizing with a wet pulverization method.
  • Formulation Example 5 10 parts of the condensed heterocyclic compounds 1-131, 2 parts of the carboxamide compound (2a), 1.5 parts of sorbitan trioleate, and 28 parts of an aqueous solution containing 2 parts of polyvinyl alcohol are mixed and wet pulverized. After finely pulverizing by the method, an aqueous solution containing 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate is added to make the total amount 90 parts, and further 10 parts of propylene glycol is added and mixed by stirring. obtain.
  • Formulation Example 6 10 parts of the condensed heterocyclic compounds 1-131, 2 parts of the carboxamide compound (2e), 1.5 parts of sorbitan trioleate, and 28 parts of an aqueous solution containing 2 parts of polyvinyl alcohol are mixed and wet pulverized. After finely pulverizing by the method, an aqueous solution containing 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate is added to make 90 parts in total, and 10 parts of propylene glycol is further added and stirred and mixed. obtain.
  • Formulation Example 7 Of the condensed heterocyclic compounds 1-131, 10 parts of one kind, 10 parts of the present carboxamide compound (2a), 3 parts of calcium lignin sulfonate, 2 parts of sodium lauryl sulfate, and the remainder of the synthetic silicon hydroxide are thoroughly mixed. To obtain 100 parts of each wettable powder.
  • Formulation Example 8 Of the condensed heterocyclic compounds 1-131, 10 parts of one kind, 10 parts of the carboxamide compound (2e), 3 parts of calcium lignin sulfonate, 2 parts of sodium lauryl sulfate, and the remainder of the synthetic silicon hydroxide are well pulverized and mixed. To obtain 100 parts of each wettable powder.
  • Formulation Example 9 1 part of the present condensed heterocyclic compounds 1-131, 0.5 part of the present carboxamide compound (2a), 1 part of synthetic silicon hydroxide fine powder, 2 parts of calcium lignin sulfonate, 30 parts of bentonite and kaolin clay Add the remainder and mix. Next, an appropriate amount of water is added to the mixture, and the mixture is further stirred, granulated by a granulator, and dried by ventilation to obtain each granule.
  • Formulation Example 10 1 part of the present condensed heterocyclic compounds 1-131, 0.5 part of the present carboxamide compound (2e), 1 part of synthetic silicon hydroxide fine powder, 2 parts of calcium lignin sulfonate, 30 parts of bentonite and kaolin clay Add the remainder and mix. Next, an appropriate amount of water is added to the mixture, and the mixture is further stirred, granulated by a granulator, and dried by ventilation to obtain each granule.
  • Test example 1 This condensed heterocyclic compound 3, 23, 27, 31, 39, 41, 42, 46, 48, 51, 56, 58, 64, 69, 72, 74, 78, 83, 91, 97, 104, 105, 107 , 108, 109, 118, 119, 120, 127, 130 and 131, xylene, dimethylformamide and surfactants (product names: Solpol 3005X, Toho Chemical Industries, respectively) having a volume ratio of 4: 4: 1, respectively, per mg. And then diluted with water containing 0.02% by volume of a spreading agent (trade name: Cinderine, manufactured by Sumitomo Chemical Co., Ltd.) so as to have a predetermined concentration.
  • a spreading agent trade name: Cinderine, manufactured by Sumitomo Chemical Co., Ltd.
  • the carboxamide compound (2a) was dissolved in 10 ⁇ L of a mixed solvent of xylene, dimethylformamide, and a surfactant (trade name: Solpol 3005X, manufactured by Toho Chemical Industry), each having a volume ratio of 4: 4: 1, per 1 mg.
  • the solution was diluted with water containing 0.02% by volume of a spreading agent (trade name: Cyndyne, manufactured by Sumitomo Chemical Co., Ltd.) so as to obtain a predetermined concentration.
  • a test drug solution was prepared by mixing a water dilution of the condensed heterocyclic compound and a water dilution of the carboxamide compound (2a).
  • the harmful arthropod control composition of the present invention it becomes possible to control harmful arthropods.

Abstract

Une composition anti-organismes nuisibles utilisable dans le cadre de la lutte contre les arthropodes nuisibles contient : un composé représenté par la formule (1) [dans la formule, chaque symbole est tel que défini dans la description] ; et un composé représenté par la formule (2) [dans la formule, chaque symbole est tel que défini dans la description]. L'invention concerne, en particulier, la composition susmentionnée dans laquelle le rapport pondéral entre les teneurs en composé représenté par la formule (1) et en composé représenté par la formule (2) varie de 1 000/1 à 1/1 000. L'invention concerne, en particulier, la composition susmentionnée dans laquelle le rapport pondéral entre les teneurs en composé représenté par la formule (1) et en composé représenté par la formule (2) varie de 500/1 à 1/10. L'invention concerne également un procédé de lutte contre les arthropodes nuisibles comprenant une étape dans le cadre de laquelle une dose efficace de la composition est appliquée sur une plante, ou sur le sol dans lequel une plante est cultivée.
PCT/JP2013/066126 2012-06-15 2013-06-05 Composition anti-organismes nuisibles utilisable dans le cadre de la lutte contre les arthropodes nuisibles et procédé de lutte contre les arthropodes nuisibles WO2013187422A1 (fr)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9549559B2 (en) 2013-01-31 2017-01-24 Sumitomo Chemical Company, Limited Composition and method for controlling pests
US9723835B2 (en) 2013-01-31 2017-08-08 Sumitomo Chemical Company, Limited Pest control composition and method for controlling pest
US9854805B2 (en) 2013-01-31 2018-01-02 Sumitomo Chemical Company, Limited Composition and method for controlling pests
US9883675B2 (en) 2013-01-31 2018-02-06 Sumitomo Chemical Company, Limited Method for controlling pests
US9974307B2 (en) 2013-01-31 2018-05-22 Sumitomo Chemical Company, Limited Composition and method for controlling pests

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005505524A (ja) * 2001-07-27 2005-02-24 シンジェンタ リミテッド 殺虫剤として有用なアゾール誘導体
JP2008308448A (ja) * 2007-06-15 2008-12-25 Sankyo Agro Kk （３−硫黄原子置換フェニル）へテロアリール誘導体
WO2012086848A1 (fr) * 2010-12-24 2012-06-28 Sumitomo Chemical Company, Limited Composé hétérocyclique fusionné et son utilisation pour la lutte contre les ravageurs

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005505524A (ja) * 2001-07-27 2005-02-24 シンジェンタ リミテッド 殺虫剤として有用なアゾール誘導体
JP2008308448A (ja) * 2007-06-15 2008-12-25 Sankyo Agro Kk （３−硫黄原子置換フェニル）へテロアリール誘導体
WO2012086848A1 (fr) * 2010-12-24 2012-06-28 Sumitomo Chemical Company, Limited Composé hétérocyclique fusionné et son utilisation pour la lutte contre les ravageurs

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9549559B2 (en) 2013-01-31 2017-01-24 Sumitomo Chemical Company, Limited Composition and method for controlling pests
US9723835B2 (en) 2013-01-31 2017-08-08 Sumitomo Chemical Company, Limited Pest control composition and method for controlling pest
US9854805B2 (en) 2013-01-31 2018-01-02 Sumitomo Chemical Company, Limited Composition and method for controlling pests
US9883675B2 (en) 2013-01-31 2018-02-06 Sumitomo Chemical Company, Limited Method for controlling pests
US9974307B2 (en) 2013-01-31 2018-05-22 Sumitomo Chemical Company, Limited Composition and method for controlling pests

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