KR920006300A - 오르토-치환 페닐아세트아미드 - Google Patents

오르토-치환 페닐아세트아미드 Download PDF

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KR920006300A
KR920006300A KR1019910016559A KR910016559A KR920006300A KR 920006300 A KR920006300 A KR 920006300A KR 1019910016559 A KR1019910016559 A KR 1019910016559A KR 910016559 A KR910016559 A KR 910016559A KR 920006300 A KR920006300 A KR 920006300A
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alkyl
phenyl
group
alkenyl
alkoxy
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KR1019910016559A
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KR100188986B1 (ko
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브란트 지그베르트
암메르만 에베르하르트
로렌쯔 기젤라
사우터 후베르트
오베르도르프 클라우스
카르도르프 우베
쿠에나스트 크리스토프
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바르쯔, 스타인호프
바스프 악티엔게젤샤프트
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
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    • C07C251/24—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to carbon atoms of six-membered aromatic rings
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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Abstract

내용 없음

Description

오르토-치환 페닐아세트아미드
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 하기 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치환제를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R1이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  2. 제1항에 있어서, R2및 R2이 각각 수소인 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드.
  3. 제1항에 있어서, R2, R3및 R5이 각각 수소이고, R4가 메틸이고, W가 메톡시아미노 또는 메톡시메틸렌인 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드.
  4. 제1항에 있어서, R1이 할로페닐, C1-C4-아킬레닐, 디-(C1-C4)-알킬페닐 또는 벤조티아졸-2-일이고, R2및 R3이 각각 수소이고, W가 C1-C4-알콕시아미노인 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드.
  5. 하기 일반식(Ⅱ)의 페닐아세트산 유도체를 염기의 존재 또는 부재하에 일반식(Ⅲ)의 아민과 바능시키는 것으로 이루어진 하기 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드의 제조 방법.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한체를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, L은 할로겐 또는 C1-C4-알콕시이며, 단, R1이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  6. 하기 일반식(Ⅳ)의 페닐아세토닐트릴을 산 또는 염기의 존재하에 가수분해시키고, 필요한 경우, 생성물을 아미드 질소상에서 1또는 2회 알킬화시키는 것으로 이루어진, 하기 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드의 제조 방법.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한제를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬 Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R1이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  7. 액상 또는 고상 담체 및 1종 이상의 하기 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드를 함유하는 살진균제.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한체를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R1이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  8. 불활성 담체 및 1종 이상의 하기 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드를 함유하는 살충제.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한체를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R1이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  9. 진균, 진균에 감염될 우려가 있는 식물, 이들의 서식지 또는 감염될 우려가 있는 식물의 종자를 살진균 유효량의 하기 일반식(Ⅰ)의 오르토-치환 페니라아세트아미드에 노출시키는 것으로 이루어진 진균의 억제방법
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한체를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
  10. 곤충, 선충 및(또는)진드기 또는 이들의 서식지를 살충, 살선충 또는 살선충 또는 살비 유효량의 일반식(Ⅰ)의 오르토-치환 페닐아세트아미드에 노출시키는 것으로 이루어진 해충의 억제방법.
    상기 식중, R1은 수소 C1-C18-알킬; 3개의 할로겐 원자, 3개의 C1-C4-알킬기, 부분 또는 완전할로겐화 C1-C4-알케닐기, 및 1또는 2개의 할로겐 원자 및(또는) 1개의 C1-C4-알킬기 및(또는)1개의 C1-C4-알콕시기를 가질수 있는 페닐기로 이루어진 군으로부터 선택되는 1내지 3개의 치한체를 가질수 있는 C3-C8-시클로알킬; C2-C10-알케닐, 페닐기를 가질수 있는 C2-C4-알키닐; C1-C4-알콕시-C1-C4-알킬, C1-C4-알콕시 카르보닐; 각 방향족 고리가 2개의 니트로기, 2개의 시아노기, 5개의 할로겐 원자 및 각각의 경우에 있어서, C1-C4-알킬, 부분 또는 완전 할로겐화 C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐 및 C1-C4-알콕시 중 3개, 및 1개의 페닐, 벤질, 페녹시 벤질옥시 또는 페닐티오기(여기서, 마지막 두 기는 시아노, 할로겐 또는 C1-C4-알킬 중 1내지 2개를 가질수 있음)로 이루어진 군으로부터 선택되는 치환체를 1내지 5개 가질수 있는 페닐, 페닐-C1-C4-알킬, 페닐-C2-C4-알케닐 또는 페녹시-C1-C4-알킬; 2개의 인접 산소 및(또는) 황원자를 갖는 복소환을 제외하고, 2개의 산소, 2개의 황 및 3개의 질소 원자로 이루어진 군으로 부터 선택되는 1 내지 3개의 헤텔 원자를 가지며, 벤젠 고리 또는 1개의 질소, 산소 또는 황원자를 갖는 5-또는 6원 헤테로방향족 고리가 복소환에 융합될수 있고, 이 복소환은 1개의 할로겐 원자, 1 또는 2개의 C1-C4-알킬기 또는 1개의 페닐기를 가질수 있는, 5- 또는 6원 복소환이고; R2및 R3은 각각 서로 독립적으로 수소, 시아노, 할로겐, C1-C4-알킬 또는 C1-C4-알콕시이고; R4및 R5는 각각 서로 독립적으로 수소 또는 C1-C4-알킬이거나 또는 이들중 하나는 C1-C4-알콕시이고; Y는 산소, 황; -SO-, -SO2-, -CH2-O-SO2-, -N=N-, -O-CO, -CO-O 또는 -CO-O-CH2-; 부분 또는 완전 할로겐화될수 있고, 시아노, 니트로, C1-C4-알킬, 부분 또는 완전 할로겐화, C1-C4-알킬, C2-C4-알케닐, 부분 또는 완전 할로겐화 C2-C4-알케닐, C1-C4-알콕시, 및 시아노, 할로겐 또는 C1-C4-알킬 중 1 또는 2개를 가질수 있는 페닐 또는 페녹시중 1개를 가질수 있는 C1-C4-알킬렌; C2-C4-알케닐렌, C2-C4-알키닐렌, 옥시(C1-C4)-알킬렌, 티오-(C1-C4)-알킬렌, C1-C4-알킬렌옥시 또는 카르보닐-(C1-C4)알킬렌, C1-C4-알킬렌카르보닐 또는 카르보닐옥시-(C1-C4)-알킬렌이고; W는 C1-C4-알콕시이미노, C1-C4-알콕시메틸렌 또는 C1-C4-알킬티오메틸렌이며, 단, R이 수소, 페닐 또는 2,2-디메틸-3-(2,2-디클로로비닐)시클로프로필이고, R2내지 R5이 각각 수소이고, Y가 카르보닐옥시메틸렌이고, W가 메톡시메틸렌 또는 메틸티오메틸렌인 화합물은 제외한다.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910016559A 1990-09-22 1991-09-20 오르토-치환 페닐아세트아미드 KR100188986B1 (ko)

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HU913023D0 (en) 1992-01-28
AU8465691A (en) 1992-03-26
IL99113A (en) 1995-11-27
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ATE156478T1 (de) 1997-08-15
ATE130598T1 (de) 1995-12-15
SK280714B6 (sk) 2000-06-12
JP3388765B2 (ja) 2003-03-24
KR100188986B1 (ko) 1999-06-01
DE4030038A1 (de) 1992-03-26
CA2049162C (en) 2004-01-13
DK0669315T3 (da) 1997-09-15
US5523454A (en) 1996-06-04
HUT58691A (en) 1992-03-30
US5677347A (en) 1997-10-14
EP0477631A1 (de) 1992-04-01
CZ293591B6 (cs) 2004-06-16
HU211029B (en) 1995-09-28
DE59106935D1 (de) 1996-01-04
EP0669315B1 (de) 1997-08-06
US5395854A (en) 1995-03-07
ZA917510B (en) 1993-03-22
CS287291A3 (en) 1992-04-15
ES2106593T3 (es) 1997-11-01
EP0669315A1 (de) 1995-08-30
CA2049162A1 (en) 1992-03-23
AU637527B2 (en) 1993-05-27
GR3024520T3 (en) 1997-11-28
IL99113A0 (en) 1992-07-15
EP0477631B1 (de) 1995-11-22
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US5516804A (en) 1996-05-14

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