KR900006304A - 치환된 1,3,5- 트리아진트리온, 이의 제조방법 및 구충제로서의 이의 용도 - Google Patents

치환된 1,3,5- 트리아진트리온, 이의 제조방법 및 구충제로서의 이의 용도 Download PDF

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KR900006304A
KR900006304A KR1019890014437A KR890014437A KR900006304A KR 900006304 A KR900006304 A KR 900006304A KR 1019890014437 A KR1019890014437 A KR 1019890014437A KR 890014437 A KR890014437 A KR 890014437A KR 900006304 A KR900006304 A KR 900006304A
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triazinetrione
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린트네르 베르네르
하베르코른 악셀
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요아힘 그렘, 클라우스 대너
바이엘 아크티엔게젤샤프트
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Abstract

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치환된 1,3,5-트리아진트리온, 이의 제조방법 및 구충제로서의 이의 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (17)

  1. 일반식(I)의 치환된 1,3,5-트리아진트리온.
    상기식에서, R1은 각각 임의로 치환된 방향족 또는 헤테로 방향족 래디칼이며, R2는 수소 또는 각각 임의로 치환된 알킬, 알케닐, 알키닐 또는 아르알킬이고, R3은 수소, 할로겐 알킬, 할로게노알킬, 알콕시, 알킬티오, 할로게노알콕시, 할로게노알킬티오, 시아노, 알콕시카보닐, 알킬설포닐 및 할로게노알킬설포닐을 포함하는 그룹 중에서 선택된 하나 이상의 동일하거나 상이한 래디칼이며, R4는 수소, 또는 각각 임의로 치환된 직쇄, 측쇄 또는 사이클릭알킬, 알케닐, 알키닐, 아르알킬 또는 아릴이고, R5는 수소, 또는 임의로 치환된 알킬, 알케닐, 알키닐 또는 아르알킬이다.
  2. (a) 일반식(Ⅱ)의 화합물을 일반식(Ⅲ)의 치환된 카보닐 이소시아네이트와 반으시키거나, (b) 일반식(Ⅱ)의 화합물을 , 경우에 따라 산수용체의 존재하에서, 일반식(Ⅳ)의 화합물과 반응시키거나, (c) 일반식(Ⅴ)의 화합물을, 경우에 따라 염기의 존재하에서, 일반식(Ⅵ)의 화합물과 반응시키거나, (d) 일반식(Ia)의 화합물을 일반식(Ⅶ)의 화합물과 반응시킴을 특징으로 하여, 일반식(I)의 치환된 1,3,5-트리아진트리온을 제조하는 방법.
    상기식에서, R1,R2,R3,R4및 R5는 제 1 항에서 정의한 바와같고, 단 일반식(Ⅶ)에 있어서, R5는 임의로 치환된 알킬, 알케닐, 알키닐 및 아르알킬이며, R6은 할로겐 원자, 알콕시 그룹 또는 아릴옥시 그룹이고, R7은 수소 또는 알킬 그룹이며, R8및 R9는 알콕시 그룹이고, A는 할로겐, OSO2, 알킬, OSO2-아릴 및 OSO2-할로게노알킬 그룹이다.
  3. 일반식(Ⅱ)의 화합물.
    상기식에서, R1,R2,R3및 R4는 제 1 항에서 정의한 바와 같다.
  4. (a) 일반식(Ⅷ)의 화합물을 일반식(Ⅸ)의 이소시아네이트와 반응시키거나, (b) 일반식(Ⅹ)의 화합물을 일반식(XI)의 화합물과 반응시킴을 특징으로 하여, 제 3 항에 따른 일반식(Ⅱ)의 화합물을 제조하는 방법.
    상기식에서, R1,R2,R3및 R4는 제 1 항에서 정의한 바와 같다.
  5. 일반식(V)의 화합물.
    상기식에서, R1,R2,R3및 R4는 제 1 항에서 정의한 바와 같다.
  6. 제 2 항에 따른 일반식(Ⅱ)의 화합물을 포스겐 및 암모니아와 반응시킴을 특징으로 하여, 제 5 항에 따른 일반식(V)의 화합물을 제조하는 방법.
    상기식에서, R1,R2,R3및 R4는 제 1 항에서 정의한 바와 같다.
  7. 일반식(Ⅷ)의 화합물.
    상기식에서, R1은 티오펜을 제외한 헤테로 방향족 래디칼, 또는 할로겐알킬티오 또는 할로겐알콕시에 의해 치환된 페닐 그룹이며, R2및 R3은 제 1 항에서 정의한 바와 같다.
  8. 일반식(Ⅶ)의 화합물을 수소화시킴을 특징으로 하여, 제 7 항에 따른 일반식(Ⅷ)의 화합물을 제조하는 방법.
    상기식에서, R1,R2및 R3는 제 7 항에서 정의한 바와 같다.
  9. 일반식(X)의 화합물.
    상기식에서, R1,R2및 R3은 제 4 항에서 정의한 바와 같다.
  10. 일반식(Ⅷ)의 화합물을 포스겐과 반응시킴을 특징으로 하여, 제 9 항에 따른 일반식(X)의 화합물을 제조하는 방법.
    상기식에서, R1,R2및 R3은 제 4 항에서 정의한 바와 같다.
  11. 일반식(Ⅶ)의 화합물.
    상기식에서, R1,R2및 R95제 7 항에서 정의한 바와 같다.
  12. 일반식(Ⅷ)의 화합물을 일반식(XIV)의 화합물과 반응시킴을 특징으로 하여, 제 11항에 따른 일반식(Ⅶ)의 화합물을 제조하는 방법.
    상기식에서, R1,R2및 R3은 제 7 항에서 정의한 바와 같으며, A는 할로겐이다.
  13. 제 1 항에 따른 일반식(Ⅰ)의 1,3,5-트리아진트리온을 하나 이상 함유함을 특징으로 하는 구충제.
  14. 기생충을 제거하기 위한 제 1 항에 따른 일반식(Ⅰ)의 1,3,5-트리아진트리온의 용도.
  15. 제 1 항에 따른 일반식(Ⅰ)의 1,3,5-트리아진트리온을 기생충 및/또는 이의 서식처에 작용시킴을 특징으로 하여, 기생충을 제거하는 방법.
  16. 제 1 항에 따른 일반식(Ⅰ)의 1,3,5-트리아진트리온을 중량제 및/또는 계면 활성제와 혼합시킴을 특징으로 하여, 구충제를 제조하는 방법.
  17. 구충제를 제조하기 위한 제 1 항에 따른 일반식(Ⅰ)의 1,3,5-트리아진트리온의 용도.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890014437A 1988-10-08 1989-10-07 치환된 1,3,5- 트리아진트리온, 이의 제조방법 및 구충제로서의 이의 용도 KR900006304A (ko)

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US6254824B1 (en) * 1998-08-27 2001-07-03 Scott Fly Rod Company Method for controlling myxobolus cerebralis
CN1189175C (zh) 1998-10-08 2005-02-16 高新研究公司 用于预防和治疗原虫病的组合物和方法
US6150361A (en) * 1998-12-22 2000-11-21 Bayer Corporation Triazineone compounds for treating diseases due to sarcosystis, neospora and toxoplasma
US6194408B1 (en) * 1998-12-22 2001-02-27 Bayer Corporation Triazineone compounds for treating diseases due to Sarcocystis, Neospora and Toxoplasma
DE19958388A1 (de) * 1999-12-03 2001-06-07 Bayer Ag Triazinonverbindungen zur Behandlung von durch den Befall mit parasitischen Protozoen bedingten Krankheiten
EP1110957A1 (en) * 1999-12-24 2001-06-27 Applied Research Systems ARS Holding N.V. Benzazole derivatives and their use as JNK modulators
US6429211B1 (en) 2000-05-23 2002-08-06 Bayer Corporation Praziquantel compounds for treating diseases due to Sarcocystis Neospora Toxoplasma and Isospora
MA52415A (fr) 2018-02-26 2021-01-06 AlzeCure Pharma AB Dérivés de triazine pour le traitement de maladies associées à des neurotrophines
GB201810668D0 (en) 2018-06-28 2018-08-15 Stiftelsen Alzecure New compounds

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ZA732906B (en) * 1972-05-24 1974-11-27 Du Pont Herbicidal triazines
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