KR890000473A - 벤조-융합된 사이클릭 화합물 - Google Patents

벤조-융합된 사이클릭 화합물 Download PDF

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KR890000473A
KR890000473A KR1019880007401A KR880007401A KR890000473A KR 890000473 A KR890000473 A KR 890000473A KR 1019880007401 A KR1019880007401 A KR 1019880007401A KR 880007401 A KR880007401 A KR 880007401A KR 890000473 A KR890000473 A KR 890000473A
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oxygen
sulfur
formula
alkyl
hydrogen
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도요히꼬 구메
도시오 고또
아쭈미 가모찌
아기히꼬 야나기
시게끼 야기
가쭈히꼬 시부야
히로시 미야우찌
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다떼노 그 자부로
니혼 도꾸슈 노야꾸 세이쪼 가부시끼 가이샤
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Priority claimed from JP23106387A external-priority patent/JPS6475486A/ja
Priority claimed from JP25846287A external-priority patent/JPH01102076A/ja
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Publication of KR890000473A publication Critical patent/KR890000473A/ko

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Abstract

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Description

벤조-융합된 사이클릭 화합물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
내용 없음

Claims (10)

  1. 일반식(I)의 벤조-융합된 사이클릭 화합물 및 이의 염.
    상기식에서
    R1은 메틸이거나 하나의 R1은 다른 R1과 함께 테트라메틸렌을 형성할 수 있고,
    R2는 R3와 함께 테트라메틸렌 또는 -CH2CH=CHCH2-를 나타내며, R4는 수소, 알킬, 아실, 또는 아릴이고, Y는 산소 또는 황이며, W는또는이고, T는 산소, 황, -NH- 또는알킬이며 R4는 T와 함께 염소를 나타낼 수 있다)이고, Z는 산소 또는 황이며, X는 수소 또는 할로겐이고, n은 0 또는 I이며, R은 C3-6사이클로알킬이거나, 질소수 1 내지 3의 임의 치환된 5-원 헤테로 사이클릭 그룹 또는 임의 치환된 6-원 헤테로 방향족 그룹이다.
  2. 제1항에 있어서,
    (여기에서, R1은 메틸이거나 하나의 R1은 다른 R1과 함께 테트라메틸렌을 형성할 수 있고, R2는 R3와 함께 테트라메틸렌 또는 -CH2CH=CHCH2-를 나타내며, R4는 수소, C1-C4-알킬, C1-C4-알킬카보닐 또는 페닐이고, Y는 산소 또는 황이고, W는또는이며, T는 산소, 황, -NH- 또는C1-C4-알킬이며 R4는 T와 함께 염소를 나타낼 수 있다)이고, Z가 산소 또는 황이며, X가 수소 또는 할로겐이고, n이 0 또는 1이며, R이 C3-6사이클로알킬, 하나의 산소 원자 또는 하나의 황원자와 함께 질소수 1내지 2의, 또는 질소수 1 또는 3의 임의 치환된 5-원 헤테로 사이클릭 그룹, 또는 질소수 1 내지 3의 임의 치환된 6-원 헤테로 방향족 그룹(여기에서, 각 경우의 동일하거나 상이한 치환체는 아미노, C1-C4-알킬아미노, 디(C1-C4-알킬)아미노, 포밀아미노, C1-C4-알킬카보닐아미노, 할로겐, C1-C4-알콕시, C1-C4-알킬티오, C1-C4-알킬, 할로게노-C1-C4-알킬 및/또는 C1-C4-알콕시C1-C4-알킬이고, R이 6-원 헤테로 방향족 그룹인 경우는, 또한 이들의 염산염이다)인 일반식(I)의 벤조-융합된 사이클릭 화합물.
  3. 제1항에 있어서,
    R2는 R3와 함께 테트라메틸렌 또는-CH2CH=CHCH2-를 나타내고, R4는 수소, 메틸, 에틸, 메틸카보닐 또는 페닐이며, T는 산소 또는 황이거나, R4는 T와 함께 염소를 나타낼 수 있고, Y는 산소 또는 황이며, W는또는이다)이고, Z가 산소 또는 황이며, X가 수소 또는 불소이고, n이 0 또는 1이며, R이 사이클로프로필, 질소수 1이상 및 산소수 1 또는 황원자수 1의 임의 치환된 5-원 헤테로 사이클릭 그룹 또는 질소수 1 또는 2의 6-원 헤테로 방향족그룹(여기에서, 각 경우의 동일하거나 상이한 치환체는 아미노, 메틸아미노, 에틸아미노, 디메틸아미노, 포밀아미노, 아세트아미노, 플루오로, 클로, 브로모, 메톡시, 에톡시, 메틸티오, 에틸티오, 메틸, 에틸, 이소프로필, 트리클로로메틸, 트리플루오로메틸 및/또는 메톡시메틸이다)인 일반식(I)의 화합물.
  4. 제1항에 있어서,
    (여기에서, R2는 R3와 함께 테트라메틸렌 또는 -CH2CH=CHCH2-를 나타내고, Y는 산소 또는 황이며, W는또는이다)이고, Z가 산소 또는 황이며, X가 불소이고, n이 0 또는 1이며, R이 테트라하이드로푸란, 푸란, 티오펜, 피라졸, 이미다졸, 1,2,4-트리아졸, 테트라졸, 이소옥사졸, 옥사졸, 1,2,4-옥사디아졸, 1,2,5-옥사디아졸, 1,3,4-옥사디아졸, 이소티아졸, 티아졸, 1,2,3-티아디아졸, 1,2,4-티아디아졸, 1,2,5-티아디아졸, 1,3,4-티아디아졸, 피리딘, 피리미딘 및 피라진을 함유하는 임의 치환된 헤테로사이클릭 그룹(여기에서, 각 경우의 동일하거나 상이한 치환체는 아미노, 메틸아미노, 에틸아미노, 디메틸아미노, 포밀아미노, 아세트아미노, 플루오로, 클로로, 브로모, 메톡시, 에톡시, 메틸티오, 에틸티오, 메틸, 에틸, 이소프로필, 트리클로로메틸, 트리플루오로메틸 및 메톡시메틸이다)인 일반식(I)의 화합물.
  5. a) Q가인 경우, 일반식(II)이 화합물을 불활성 용매존재하에 일반식(III)의 화합물과 반응시키거나,
    b) Q가인 경우, 일반식(IV)의 화합물을 불활성 용매 존재하 및 필요할 경우 염기 존재하에 일반식(V)의 화합물과 반응시키거나,
    c) Q가(여기에서, R2는 R3와 함께 테트라메틸렌을 나타내며, W는또는이다)인 경우, 일반식(VI)의 화합물을 불활성 용매 존재하에 적합한 염기와 반응시키거나,
    d) Q가(여기에서, R2는 R3와 함께 -CH2CH=CHCH2=를 나타내며, W는이다)인 경우, 일반식(VII)의 화합물을 불활성 용매 존재하에 적합한 염기와 반응시키거나,
    e) Q가인 경우, 일반식(VIII)의 화합물을 불활성 용매 존재하에 염소화제와 반응시키거나,
    f) Q가인 경우, 일반식(Ia)의 화합물을 불활성 용매 존재하에 환원시키거나,
    g) Q가인 경우, 일반식(Ib)의 화합물을 불활성 용매 존재하에 염소화제와 반응시키거나,
    h) Q가(여기에서, R4는 아실이고, T는 산소이며 R4는 R5로 치환된다)인 경우, 상기 일반식(Ib)의 화합물을 불활성 용매존재하 및 필요할 경우 염기 존재하에 일반식(IX)의 화합물 또는 일반식(X)의 화합물과 반응시키거나,
    i) Q가(단, 여기에서 R4-T-는 -OH, -Cl 또는 아실옥시가 아닌 경우, R4-T-는 -OH, -Cl 또는 아실옥시가 아닌 경우, R4-T-는 R6로 치환된다)인 경우, 일반식(Ic)의 화합물을 불활성 용매 존재하 및 필요할 경우 염기 존재 하에 일반식(XI)의 화합물과 반응시킴을 특징으로 하여, 일반식(I)의 벤조-융합된 사이클릭 화합물 및 이의 염을 제조하는 방법.
    상기식에서 Q는
    (여기에서, R1은 메틸이거나 하나의 R1은 다른 R1과 함께 테트라메틸렌을 형성할 수 있고, R2는 R3와 함께 테트라메틸렌 또는 -CH1CH=CHCH1-를 나타내며, R4는 수소, 알킬, 아실 또는 아릴이고, Y는 산소 또는 황이며, W는또는알킬이며 R4는 T와 함께 염소를 나타낼 수 있다)이고, Z는 산소 또는 황이며, X는 수소 또는 할로겐이고, n은 0또는 1이며, R은 C3-6사이클로알킬이거나, 질소수 1내지 3의 임의 치환된 5-원 헤테로사이클릭 그룹 또는 임의 치환된 6-원 헤테로방향족 그룹이고, M은 할로겐, 메탄설포닐옥시, 벤질설포닐옥시 또는 P-톨루엔설포닐옥시이며, R5는 아실이고, R6은 알콕시, 알킬티오, 페녹시, 페닐티오, 알킬아미노 또는 디알킬아미노이다.
  6. 제1항 내지 5항에 따른 일반식(I)의 벤즈옥사지논 하나이상을 함유함을 특징으로 하는 제초제조성물.
  7. 제1항 내지 5항에 따른 일반식(I)의 벤즈옥사지논을 잡초 및/또는 이들의 서식지에 적용시킴을 특징으로 하여 잡초를 제거하는 방법.
  8. 잡초를 제거하기 위한 제1 내지 5항에 따른 일반식(I)의 벤즈옥사지논의 용도.
  9. 제1 내지 5항에 따른 일반식(I)의 벤즈옥사지논을 중량제 및/또는 계면활성제와 혼합시킴을 특징으로 하여, 제초제조성물을 제조하는 방법.
  10. 일반식(XIX)의 화합물.
    상기식에서, E는 수소, 니트로, 아미노, 하이드라지노, 시아네이토 또는 티오시아네이토이고, X는 수소 또는 할로겐이며, Z는 산소 또는 황이고, R은 C3-6사이클로알킬이거나, 질소수 1 내지 3의 임의 치환된 5-원 헤테로사이클릭그룹 또는 임의 치환된 6-원 헤테로방향족 그룹이며, n은 0 또는 1이다.
    ※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880007401A 1987-06-22 1988-06-20 벤조-융합된 사이클릭 화합물 KR890000473A (ko)

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JP15509387 1987-06-22
JP(?)62-155093 1987-06-22
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JP23106387A JPS6475486A (en) 1987-09-17 1987-09-17 Benzoxazinones and herbicide
JP(?)62-258462 1987-10-15
JP25846287A JPH01102076A (ja) 1987-10-15 1987-10-15 ベンゾ縮合環化合物及び除草剤

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