KR850001180A - Method for preparing an aryloxybenzoic acid derivative - Google Patents

Method for preparing an aryloxybenzoic acid derivative Download PDF

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KR850001180A
KR850001180A KR1019840004486A KR840004486A KR850001180A KR 850001180 A KR850001180 A KR 850001180A KR 1019840004486 A KR1019840004486 A KR 1019840004486A KR 840004486 A KR840004486 A KR 840004486A KR 850001180 A KR850001180 A KR 850001180A
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halogen atom
hydrogen
formula
compound
group
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KR1019840004486A
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Korean (ko)
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까르봉 브르뜨랑
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샤를르 브라소뜨
롱-쁠랑 아그로시미
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Publication of KR850001180A publication Critical patent/KR850001180A/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D257/00Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D257/04Five-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/713Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

내용 없음No content

Description

아릴옥시벤조산 유도체의 제조방법Method for preparing an aryloxybenzoic acid derivative

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (13)

하기 일반식(II)의 페닐테트라졸을 하기 일반식(III)의 화합물과 반응시킴을 특징으로 하는 하기 일반식의 화합물의 제조방법.A process for preparing a compound of the general formula (II), wherein the phenyltetrazole of the general formula (II) is reacted with a compound of the general formula (III). (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CO, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄)기를 나타내고, W는 수소 또는 할로겐원자, 또는 니트로기를 나타내고, R은 수소 또는 할로겐원자, 또는 임의 치환된 지방족, 방향족, 알킬티오, 아미노, 아실, 알킬술포닐, 아릴술포닐, 히드록시 또는 시아노기를 나타내고, A는 히드록시기 또는 할로겐원자를 나타내고, B는 할로겐원자 또는 히드록시기를 나타내며, 단, B는 A와는 다르게 선택되어야 하며 히드록시기를 함유하는 반융물은 페네이트형일 수도 있다.)Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CO, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z ) = (Wherein Z represents hydrogen or halogen atom), W represents hydrogen or halogen atom, or nitro group, R represents hydrogen or halogen atom, or optionally substituted aliphatic, aromatic, alkylthio, amino, acyl Represents an alkylsulfonyl, arylsulfonyl, hydroxy or cyano group, A represents a hydroxy group or a halogen atom, B represents a halogen atom or a hydroxy group, except that B is selected differently from A and contains a hydroxy group The melt may be phenate type.) 하기 일반식(IV)의 화합물을 할로겐화시킴을 특징으로 하는 하기 일반식(I)의 화합물의 제조방법.A process for preparing a compound of formula (I), wherein the compound of formula (IV) is halogenated. (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CN, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄)기를 나타내고, W는 할로겐원자를 나타내고, R은 수소 또는 할로겐원자, 또는 임의 치환된 지방족, 방향족, 알킬티오, 아미노, 아실, 알킬술포닐, 아릴술포닐, 히드록시 또는 시아노기를 나타낸다.)Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CN, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z ) = (Wherein Z represents hydrogen or halogen atom), W represents halogen atom, R represents hydrogen or halogen atom, or optionally substituted aliphatic, aromatic, alkylthio, amino, acyl, alkylsulfonyl, Arylsulfonyl, hydroxy or cyano groups.) 하기 일반식(IV)의 화합물을 질화시킴을 특징으로 하는 하기 일반식(A)의 화합물의 제조방법.A process for producing a compound of formula (A), wherein the compound of formula (IV) is nitrided. (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CN, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄)기를 나타내고, R은 수소 또는 할로겐원자, 또는 임의 치환된 지방족, 방향족, 알킬티오, 아미노, 아실, 알킬술포닐, 아릴술포닐, 히드록시 또는 시아노기를 나타낸다.)Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CN, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z ) = (Wherein Z represents hydrogen or a halogen atom) and R represents hydrogen or a halogen atom, or optionally substituted aliphatic, aromatic, alkylthio, amino, acyl, alkylsulfonyl, arylsulfonyl, hydroxy or Cyano group.) NaN3를 하기 일반식(IV)의 니트릴과 반융시킴을 특징으로 하는 하기 일반식(VII)의 화합물의 제조방법.A process for preparing a compound of formula (VII), characterized in that the NaN 3 is semi-melted with a nitrile of formula (IV). (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CN, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄)기를 나타낸다.Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CN, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z ) = (Wherein Z represents hydrogen or halogen atoms). 하기 일반식(IX)의 화합물을 적당한 염기, 바람직하게는 수산화나트륨과 반융시킴을 특징으로 하는 하기 일반식(IX)의 화합물의 염의 제조방법.A process for preparing a salt of a compound of formula (IX) characterized in that the compound of formula (IX) is semi-melted with a suitable base, preferably sodium hydroxide. (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CN, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄)기를 나타내고, W는 수소 또는 할로겐원자 또는 니트로기를 나타낸다.)Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CN, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z (Wherein Z represents a hydrogen or halogen atom), and W represents a hydrogen or halogen atom or a nitro group.) 하기 일반식(VIII)의 화합물을 하기 일반식(VII)의 화합물과 반응시킴을 특징으로 하는 하기 일반식(I)의 화합물의 제조방법.A process for preparing a compound of formula (I), wherein the compound of formula (VIII) is reacted with a compound of formula (VII). (상기 식중, X는 할로겐원자 또는 하나이상의 할로겐원자로 치환된 저급알킬기를 나타내고, Y는 수소 또는 할로겐원자, 또는 CF3, CN, NO2또는 CH3기를 나타내고, D는 질소원자 또는 -C(Z)=(식중, Z는 수소 또는 할로겐원자를 나타냄) 기를 나타내고, W는 수소 또는 할로겐원자, 또는 니트로기를 나타내고, R은 할로겐원자 또는 임의 치환된 지방족, 방향족, 알킬티오, 아미노, 아실, 알킬술포닐, 아릴술포닐, 히드록시 또는 시아노기를 나타내고, T는 출발기를 나타낸다.)Wherein X represents a lower alkyl group substituted with a halogen atom or one or more halogen atoms, Y represents a hydrogen or halogen atom or a CF 3 , CN, NO 2 or CH 3 group, and D represents a nitrogen atom or -C (Z ) = (Wherein Z represents hydrogen or halogen atom), W represents hydrogen or halogen atom, or nitro group, R represents halogen atom or optionally substituted aliphatic, aromatic, alkylthio, amino, acyl, alkylsul Phonyl, arylsulfonyl, hydroxy or cyano groups, and T represents a starter group.) 활성성분으로서 제1 내지 6항에 따른 화합물중 하나이상을 함유하는 제초조성물.Herbicide composition containing at least one of the compounds according to claims 1 to 6 as an active ingredient. 제7항에 있어서, 활성성분과 더불어 1종 이상의 농업적으로 수용될 수 있는 고체 또는 액체담체 및 1종이상의 농업적으로 수용될 수 있는 표면활성제를 함유하는 조성물.8. A composition according to claim 7, comprising an active ingredient together with at least one agriculturally acceptable solid or liquid carrier and at least one agriculturally acceptable surfactant. 제8항에 있어서, 0.5 내지 95%의 활성성분을 함유하는 조성물.The composition of claim 8 which contains 0.5 to 95% of active ingredient. 제9항에 있어서, 1 내지 95%의 담체 및 0.1 내지 20%의 표면활성제를 함유하는 조성물.The composition of claim 9 containing 1 to 95% of a carrier and 0.1 to 20% of a surfactant. 제1 내지 6항에 따른 활성성분중 어느 하나를 유효량 사용함을 특징으로 하는 농작물의 선택적 제초방법.Method for selective weeding of crops, characterized in that an effective amount of any one of the active ingredients according to claim 1 is used. 제11항에 있어서, 제7 내지 10항에 따른 조성물중 어느 하나를 활성성분이 0.01 내지 5㎏/ha, 바람직하게는 0.1 내지 2㎏/ha의 비율로 가해지도록 사용하는 방법.Process according to claim 11, wherein any one of the compositions according to claims 7 to 10 is used such that the active ingredient is added at a rate of 0.01 to 5 kg / ha, preferably 0.1 to 2 kg / ha. 제11 또는 12항에 있어서, 농작물이 콩류인 방법.The method of claim 11 or 12, wherein the crop is legumes. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019840004486A 1983-07-27 1984-07-27 Method for preparing an aryloxybenzoic acid derivative KR850001180A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR83-12619 1983-07-27
FR8312619A FR2549831A1 (en) 1983-07-27 1983-07-27 NOVEL ARYLOXYBENZOIC ACID DERIVATIVES AND THEIR USE AS HERBICIDES

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KR850001180A true KR850001180A (en) 1985-03-16

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KR (1) KR850001180A (en)
AU (1) AU3113484A (en)
BE (1) BE900237A (en)
BR (1) BR8403737A (en)
DD (1) DD218543A5 (en)
DE (1) DE3427606A1 (en)
FR (1) FR2549831A1 (en)
GB (1) GB2144125A (en)
GR (1) GR82227B (en)
HU (1) HUT35252A (en)
IL (1) IL72362A0 (en)
IT (1) IT1178500B (en)
LU (1) LU85477A1 (en)
MA (1) MA20184A1 (en)
NL (1) NL8402312A (en)
OA (1) OA07756A (en)
PT (1) PT78983B (en)
ZA (1) ZA845763B (en)

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HU209793B (en) * 1990-09-25 1994-11-28 Chinoin Gyogyszer Es Vegyeszet Process for the production of pyrido[1,2-a]pyrimidine-derivatives and pharmaceutical compositions containing the same
PL3083564T3 (en) 2013-12-20 2018-12-31 Novartis Ag Heteroaryl butanoic acid derivatives as lta4h inhibitors

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* Cited by examiner, † Cited by third party
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JPS5516432B2 (en) * 1974-05-28 1980-05-01
DE2613697A1 (en) * 1976-03-31 1977-10-13 Hoechst Ag HERBICIDAL AGENTS
DK155935C (en) * 1979-05-16 1989-10-16 Rohm & Haas SUBSTITUTED DIPHENYLETHERS, HERBICIDE PREPARATIONS CONTAINING THESE COMPOUNDS AND PROCEDURES TO COMBAT WEEDS
DE2933962A1 (en) * 1979-08-22 1981-03-26 Hoechst Ag, 65929 Frankfurt 2-Substd.-4,5-di:chloro-imidazole derivs. - useful as fungicides and antimycotics, prepd. by reacting aldehyde with di:cyanide and hydrogen chloride

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HUT35252A (en) 1985-06-28
IL72362A0 (en) 1984-11-30
GB8418958D0 (en) 1984-08-30
FR2549831A1 (en) 1985-02-01
AU3113484A (en) 1985-01-31
DE3427606A1 (en) 1985-02-07
IT8422035A0 (en) 1984-07-25
IT1178500B (en) 1987-09-09
BR8403737A (en) 1985-07-02
NL8402312A (en) 1985-02-18
GR82227B (en) 1984-12-13
LU85477A1 (en) 1986-02-12
GB2144125A (en) 1985-02-27
DD218543A5 (en) 1985-02-13
MA20184A1 (en) 1985-04-01
PT78983B (en) 1986-10-23
BE900237A (en) 1985-01-28
OA07756A (en) 1985-08-30
ZA845763B (en) 1985-03-27
PT78983A (en) 1984-08-01

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