KR910016729A - 살균 활성을 나타내는 아민 유도체 - Google Patents

살균 활성을 나타내는 아민 유도체 Download PDF

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KR910016729A
KR910016729A KR1019910004009A KR910004009A KR910016729A KR 910016729 A KR910016729 A KR 910016729A KR 1019910004009 A KR1019910004009 A KR 1019910004009A KR 910004009 A KR910004009 A KR 910004009A KR 910016729 A KR910016729 A KR 910016729A
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oxapropyl
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까마기 지오반니
필립피니 루치오
구스메롤리 마릴레나
가라발리아 까를로
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미니스테로 델우니베르시타 에 델라 리세르카 사이엔티피카 에 테크놀로지카
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Abstract

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Description

살균 활성을 나타내는 아민 유도체
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (18)

  1. 하기 일반식을 갖는 화합물, 그의 거울상 이성질체, 부분입체 이성질체 및 상응하는 금속염 및 착화물,
    [상기 식중 : R1및R2는 서로 동일하거나 다르고, H 원자, 직쇄 또는 측쇄(C1~C6)-알킬기, 또는 Ar-B기(상기 식중, Ar은(C6~C10)-아릴 또는 (C6~C10)-할로-아릴기이고, B는 (C1~C4)-알킬렌 또는 (C1~C2)-알킬-(C1~C4)-알킬렌기이거나, Ar및 B는 서로 및 N원자와 함께 결합하여, O및 S로 부터 선택된 제 2헤테로 원자를 포함하는 (C2~C7)-헤테로 환기 또는 (C3~C8) 헤테로 환기를 나타내며, 상기 헤테로환기는 임의로 치완된 것이다.)를 나타내며: R3및 R5는 서로 동일하거나 다르고, H원자, (C2~C3)-알킬기를 나타내거나 연결되어 직쇄 또는 측쇄(C1~C7)알킬렌기를 형성하며: m는 0내지 4의 정수이고: R4는 m이 1보다 클때, 서로 다르거나 동일할 수 있으며, 할로겐 원자, (C1~C3)-알킬기 또는 (C2~C3)-할로-알킬기를 나타내고: R',R″,는 서로 동일하거나 다를수 있으며, H,(C1~C3)-알킬기 또는 할로겐 원자를 나타내고: n은 0내지 3 범위 내에 포함된 정수이며 Y 는 -CH=CH2기, (C3~C6)-시클로알킬기, (C6~C10)-아릴기, 5- 또는 6- 원 헤테로환기를 나타내거나; 하기식의 기를 나타낸다.
    (상기 식중 C,D,E는 서로 동일하거나 다르며, H원자, (C1~C4)알킬기, (C1~C4)-할로알킬기, (C1~C4)-알콕시기, (C1~C4)-할로알콕시기, (C6~C10)-아릴기, 및 (C6~C10)-할로아릴기를 나타낸다.)].
  2. 제1항에 있어서, 상기의(C3~C6)-또는 (C2~C7)-헤테로 환기가, 치닐환체를 임의로 포함하는 모르폴린, 2,6-디메틸-모르폴린, 피페리딘, 2,6-디메틸-피페리딘, 티오모르폴린기 중에서 선택되는 화합물.
  3. 제 1또는 제2항에 있어서, Y가 피리딘, 피리미딘, 티오펜, 티아졸, 옥사졸, 이소옥사졸기, 및, 그들의 융합벤젠 고리 함유 유도체, 시클로헥실, 시클로프로필, 시클로펜틸, 시클로부틸, 1-메틸-2,2,-디클로로-시크로프로필, 트림메틸실릴, t-부틸-디메틸-실릴 및 디메틸-페닐-실라닐기를 나타내는 화합물.
  4. 제1항 내지 3항중 어느 한 항에 있어서, 상기 Ar-B기가 벤질기 및 3-페닐-이소프로필기에서 선택된 화합물.
  5. 제1항 내지 4항중 어느 한항에 있어서, 상기의 (C3~C8)-또는 (C2~C7)-헤테로환기가, (C1~C4)-알킬, (C6~C10)-아릴, Ar-B기(기호는 상기 정의와 동일한 의미를 가진다.), 및 할로겐 원자 중에서 선택한 적어도 하나의 기에 의해 치환된 화합물.
  6. 제1항 내지 5항 중 어느 한 항에 있어서, 에테닐, (C3~C8)-시클로알킬, 또는 헤테로환기인 상기 Y기가 할로겐 원자, (C1~C4)-알킬기, (C1~C2)-할로알케닐기, (C1~C3)-알콕시기, (C1~C3)-할로알콕시기에서 선택된 적어도 하나의 기로 치환된 화합물.
  7. 제1항에 있어서, 4-{3-[4-(트리메틸실릴메특시)페닐]-2-메틸-3-옥사프로필]-2,6-디메틸-모르폴린인 화합물.
  8. 제1항에 있어서, 4-{3-[3-(2-(4,6-디클로로)-피리딜옥시)페닐]- ]-2,6-디메틸-모르폴린인 화합물.
  9. 제1항에 있어서, 4-{3-[3-(2,2-디클로로-1-메틸-시크로프로필메톡시)페닐]-]-2-메틸-3-옥사프로필}-2,6-디메틸-모르폴린인 화합물.
  10. 제1항에 있어서, 4-[3-(5-트리플루오로메틸피리딜옥시-2-일)페닐-2-메메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  11. 제1항에 있어서, 4-[3-(3-클로로-5-트리플루오로메틸피리딜옥시-2-일)페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  12. 제1항에 있어서, 4-[4-(디메틸페닐실릴메톡시)-페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  13. 제1항에 있어서, 4-[3-(디메틸페닐실릴메톡시)-페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  14. 제1항에 있어서, 4-[3-[1-(트리메틸실릴)에톡시)페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  15. 제1항에 있어서, 4-[4-[1-(트리메틸실릴)- 에톡시)페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  16. 제1항에 있어서, 4-[3-[1-(트리메틸실릴)에톡시)페닐-2-메틸-3-옥사프로필]-2,6-디메틸모르폴린인 화합물.
  17. 하기 일반식(Ⅱ)의 카르보닐 화합물을, 하기 일반식(Ⅲ)의 아민 첨가후에, 수소화 촉매의 존재하에, 0℃내지 60℃ 범위내에 포함되는 온도에서, 1내지 10기압의 범위 내에 포함되는 수소압으로 수소화하여 하기 일반식(Ⅳ)의 아민을 수득하고, 아민(Ⅳ)를 염기 존재하에, 쌍극성 양성자성 또는 비양성자성 용매 중에서, 25℃ 내지 반응 혼합물의 비등 온도까지의 범위 내에 포함되는 온도에서 하기 일반식(Ⅴ)의 화합물과 반응시켜 화합물(Ⅰ)을 수득하고, 상기 화합물(Ⅰ)로 부터 그의 상응하는 금속염 및 착물을 통상적인 방법에 따라 제조할 수 있음을 특징으로 하는, 제 1항 내지 16항중 어느 한항에서 정의된 화합물의 제조방법.
    G-(CR'R″)-Y (V)
    [상기 식들중, G는 GI,Br, I메탄-슬포네이트 에스테르, p-톨루엔-슬포네이트 에스테르이며, 나머지 기호는 제 1항에서 정의한 의미를 가진다.]
  18. 유용식물의 경작시에 병원체 균의 성장을 억제하는, 특히 에리시페(Erysiphe)및 헬민토스포리움(Helminthosprium)속에 속하는 균을 퇴치하기 위한 억제제로서, 제1항 내지 9항중 어느 한 항에 따른 아릴-프로필-아민 화합물의 용도.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910004009A 1990-03-13 1991-03-13 살균 활성을 나타내는 아민 유도체 KR100193159B1 (ko)

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