KR910007900A - 치환된 티아졸 및 살균제로서의 이용 - Google Patents

치환된 티아졸 및 살균제로서의 이용 Download PDF

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KR910007900A
KR910007900A KR1019890017339A KR890017339A KR910007900A KR 910007900 A KR910007900 A KR 910007900A KR 1019890017339 A KR1019890017339 A KR 1019890017339A KR 890017339 A KR890017339 A KR 890017339A KR 910007900 A KR910007900 A KR 910007900A
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compound
halo
halomethyl
trifluoromethyl
methyl
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KR1019890017339A
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KR920001764B1 (ko
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홀스트 알트 게르하드
게리 필립스 웬델
캐네디 프라트 존
한나 스로우지 가브리엘
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아놀드 하비 콜
몬산토캄파니
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/30Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • 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
    • A01N43/72Biocides, 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
    • A01N43/74Biocides, 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
    • A01N43/781,3-Thiazoles; Hydrogenated 1,3-thiazoles

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Environmental Sciences (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Pest Control & Pesticides (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)
  • Float Valves (AREA)
  • Prostheses (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

내용 없음.

Description

치환된 티아졸 및 살균제로서의 이용
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (26)

  1. 다음 구조식을 갖는 화합물:
    이 구조식에서 R은 할로, 할로메틸, 1-할로에틸, 할로메톡시, 1-할로에톡시, 할로메틸티오, 1-할로에틸티오, 펜타플루오로설퍼, 할로메틸 설피닐, 1-할로에틸설피닐, 할로메틸설포닐, 1-할로에틸설포닐, R1, R2중 적어도 한 개가 할로메틸이면 R1, R2는 메틸, 에틸, 할로메틸, n은 1 내지 5의 정수가 가능하다. 또는 농격학적으로 이용가능한 그의 염이다.
  2. 제1항에 있어서, R1이 메틸인 화합물.
  3. 제2항에 있어서, R2가 트리할로메틸인 화합물.
  4. 제3항에 있어서, R2가 트리플루오로메틸인 화합물.
  5. 제4항에 있어서, 각 R이 할로, 할로메틸, 할로메톡시인 화합물.
  6. 제5항에 있어서, 각 R이 클로로, 브로모, 요오드, 트리할로메틸, 트리할로메톡시인 화합물.
  7. 제5항에 있어서, 각 R이 클로로, 브로모, 트리플로로메틸, 트리플로로메톡시인 화합물.
  8. 제6항에 있어서, n이 3,4인 화합물.
  9. 다음 구조식을 갖는 화합물.
    이 구조식에서 X는 할로, 트리할로메틸, 트리할로메톡시, Y는 할로, 트리할로메톡시, 니트로, 시아노가 각 Z는 할로, 트리할로메틸, 트리할로메톡시, 니트로, 시아노가 n은 0 내지 3의 정수가 가능하다. 또는 농경학적으로 이용가능한 그의 염이다.
  10. 제9항에 있어서, X가 할로, 트리플루오로메틸, 트리플루오로메톡시이고, Y가 할로, 트리플루오로메틸, 트리플루오로 메톡시, 니트로, 시아노이며, 각 Z는 할로, 트리플루오로메틸, 트리플루오로메톡시, 니트로, 시아노이다.
  11. 제10항에 있어서, n이 1,2인 화합물.
  12. 다음 구조식이 화합물;
    이 구조식에서 각 A는 할로, 트리플루오로메틸, 트리플루오로메톡시가 가능하고, 또는 농경학적으로 이용가능한 그의 염이다.
  13. 다음 구조식의 화합물;
    이 구조시계서 각 B는 할로, 트리플루오로메틸, 트리플루오로메톡시가 가능하고, 또는 농경학적으로 이용가능한 그의 염이다.
  14. 다음 구조식을 갖는 화합물:
    이 구조식에서 각 R에는 할로, 할로메틸, 1-할로에틸, 할로메톡시, 1-할로에톡시, 펜타플루오로설퍼, 할로메틸설피닐, 1-할로에틸설피닐, 할로메틸설포닐, 1할로에틸설포닐, 니트로, 시아노, 메틸티노, 에틸티노, 할로메틸티노, 1-할로에틸피노, 메틸설피닐, 에틸설피닐,메틸설포닐, 탄소수가 적은 알킬, 탄소수가 적은 알콕시, 탄소수가 적은 알킬카르보닐, 탄소수가 적은 알콕시카르보닐이 가능하고, R1,은 메틸, 에틸, R2는 할로메틸, n은 1내지 5의정수가 가능하며 또는 농경학적으로 이용가능한 그의 염이다.
  15. 다음 구조식을 갖는 화합물이 효과적인 살균력을 갖기 위한 양을 이루는 조성.
    각 R은 독립적으로 할로, 할로메틸, 1-할로에틸, 할로메톡시, 1-할로에톡시, 할로메틸티오, 1-할로에틸티오, 펜타플루오로설퍼, 할로메틸설피닐, 1-할로에틸설피닐, 할로메틸설포닐, 또는 1-할로에틸설포닐이고, 적어도 R1또는 R2가 할로메틸티오이면 R1및 R2는 독립적으로 메틸, 에틸 또는할로메틸이며, n은 1 내지 5의 정수이다. 또는 농격학적으로 이용가능한 그의 염.
  16. 제15항에 있어서 R1이 메틸인 화합물.
  17. 제16항에 있어서 R2가 트리할로메틸인 화합물.
  18. 제17항에 있어서 R2가 트리플루오로메틸인 화합물.
  19. 제18항에 있어서 R이 클로로, 브로모, 요오드, 트리플루오로메틸, 트리플루오로메톡시인 화합물.
  20. 제19항에 있어서 각 n이 3 또는 4인 화합물.
  21. 아래의 구조식을 갖는 화합물의 유효량을 식물 궤적(plant locus)에 도포하면서, 식물에서 곰팡이 병의 성장을 조절하는 방법:
    이 구조식에서 각 R은 할로, 할로메틸, 1-할로에틸, 할로메톡시, 1-할로에톡시, 할로메틸티오, 1-할로에틸티오, 펜타플루오로설퍼, 할로메틸설피닐, 1-할로에틸설피닐, 할로메틸설포닐, 1-할로에틸설포닐, R1, R2중 적어도 한 개가 할로메틸이면 R1과 R2는 메틸, 에틸, 할로메틸이. n은 1 내지 5의 정수가 가능하며 또한 농경학적으로 이용가능한 그의 염이다.
  22. 제21항에 있어서 R1이 메틸인 경우의 방법.
  23. 제22항에 있어서 R2가 트리할로메틸인 경우의 방법.
  24. 제23항에 있어서 R2가 트리플루오로메틸인 경우의 방법.
  25. 제24항에 있어서 R이 클로로, 브로모, 트리플로로메틸, 트리플로로메톡시인 경우의 방법.
  26. 제25항에 있어서 n이 3 또는 4인 경우의 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890017339A 1988-11-29 1989-11-28 치환된 티아졸 및 살균제로서의 이용 KR920001764B1 (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US27737588A 1988-11-29 1988-11-29
US277,375 1988-11-29
US07/414,667 US5045554A (en) 1988-11-29 1989-10-03 Substituted thiazoles and their use as fungicides
US414,667 1989-10-03

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KR920001764B1 KR920001764B1 (ko) 1992-03-02

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EP (1) EP0371950B1 (ko)
JP (1) JPH02184680A (ko)
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CN (1) CN1021010C (ko)
AT (1) ATE116973T1 (ko)
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CA (1) CA2004013C (ko)
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ES2017611A4 (es) 1991-03-01
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NO894738D0 (no) 1989-11-28
IL92482A0 (en) 1990-08-31
PT92419B (pt) 1996-06-28
PT92419A (pt) 1990-05-31
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YU225089A (en) 1991-04-30
CA2004013C (en) 1999-07-27
IN170285B (ko) 1992-03-07
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EP0371950A2 (en) 1990-06-06
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BR8906011A (pt) 1990-06-19
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