KR870010011A - 치환된 2,4-디아미노-5-시아노 피리미딘 - Google Patents
치환된 2,4-디아미노-5-시아노 피리미딘 Download PDFInfo
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- KR870010011A KR870010011A KR870004197A KR870004197A KR870010011A KR 870010011 A KR870010011 A KR 870010011A KR 870004197 A KR870004197 A KR 870004197A KR 870004197 A KR870004197 A KR 870004197A KR 870010011 A KR870010011 A KR 870010011A
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Abstract
Description
Claims (16)
- 하기 일반식(Ⅰ)의 화합물 또는 그의 염.상기 식에서,R1이 수소, C1-C6알킬, C2-C6알켄일 또는 C2-C6알킨일이고,R2가 수소, C1C10알킬, 또는 C3-C6시클로알킬이거나, 또는 R1및 R2를 합쳐서 -(CH2)3-,-(CH2)4및 -(C)5로 구성된 군으로부터 선정된 라디칼이며 ;R3가 수소 또 -CO-R5또는 -SO2-R6라디칼이고 ;R4는으로 구성된 군으로부터 선정된 라디칼이며,R5는 수소, C1-C12알킬, C3-C6시클로알킬, C1-C6알콕시, 과할로겐화 C1-C3알킬 또는라디칼이고,R6는 C1-C6알킬이며 ;R7는 수소 또는 C1-C6알킬이고 ;R8및 R9는 각각 독립적으로 수소 또는 C1-C6알킬, 또는 R8및 R9를 합쳐서 -(CH2)3, -(CH2)4- 및 -(CH2)5로 구성된 군으로부터 선정된 라디칼이며 ;라디칼이고 ;R11및 R12는 각각 독립적으로 수소 또는 C1-C6알킬 또는, R11및 R12를 합쳐서 -(CH2)3, -(CH2)4및 -(CH2)5로 구성된 군으로부터 선정된 라디칼이며 ;R13은 C1-C10알킬, 10개까지의 할로겐 원자가 치환된 C1-C10알킬 또는 C3-C6시클로 알킬이고 ;R14및 R15는 각각 독립적으로 C1-C10알킬이고 ; 또는X 및 Y는 각각 독립적으로 산소 또는 유황임.
- 제1항에 있어서,R1이 수소 또는 C1-C4알킬이고,R2가 C1-C4알킬 또는 C3-C6시클로알킬이거나, 또는R1및 R2를 합쳐서 -(CH2)4- 또는 -(CH2)5- 라디칼이며 ;R3이 수소이고 ;R4가 -NH2또는 -NH-CO-R5라디칼이며 ;R5가 C1-C4알킬 또는 과할로겐화 C1-C3알킬인 일반식 (Ⅰ)의 화합물 또는 그의 염.
- 제2항에 있어서,R1이 수소, 메틸 또는 에틸이고,R2가 C1-C4알킬 또는 시클로프로필이며,R3가 수소이고,R4가 -NH2또는 -NH-CO-R5라디칼이며,R5가 C1-C3알킬인 일반식 (Ⅰ)의 화합물 또는 그의 염.
- 제3항에 있어서,R1이 수소, 메틸 또는 에틸이고,R2가 시클로프로필이며,R3는 수소이고, 또R4는 - NH2또는 -NH-C0- C2H5라디칼인 일반식(Ⅰ)의 화합물 또는 그의 염.
- 제4항에 있어서, 하기 일반식의 화합물.
- 제4항에 있어서, 하기 일반식의 화합물.
- 제4항에 있어서, 하기 일반식의 화합물,
- 제4항에 있어서, 하기 일반식의 화합물.
- 하기 일반식(Ⅱ) 화합물을 암모니아와 반응시키거나, 또는 하기 일반식(Ⅲ) 화합물을 하기 일반식(Ⅳ) 아민과 반응시키고, 또 필요한 경우 R3가 수소이고 또 R4가 -NH2라디칼인 일반식(Ⅰ)의 수득 화합물을 이미 공지된 방법으로 R3가 -CO-R5또는 -SO2-R|6이고 및/또는 R4가인 일반식(Ⅰ)화합물로 전환시키고, 또 필요한 경우, 일반식(Ⅰ)의 수득 화합물을 그의 염으로 전환시키는 방법을 포함하는 제1항 또는 제8항 중 어느 하나에서 청구된 일반식 (Ⅰ) 화합물의 제조방법.상기 식에서,R1내지 R15,X 및 Y는 제1항에서 정의한 바와 같고, 또 n은 0,1 또는 2이다.
- 하기 일반식 (Ⅱ)의 화합물.상기 식에서,R1이 수소, C1-C6알킬, C2-C6알켄일 또는 C2-C6알킨일이고,R2가 수소, C1-C10알킬 또는 C3-C6시클로알킬이거나, 또는R1및 R2를 합쳐서, -(CH2)4- 또는 -(CH2)5- 라디칼이며 ; 또 n은 0,1 또는 2임.
- 하기 일반식(Ⅶ)의 화합물을 염소로서 산화시켜 하기 일반식(ⅩⅢ)의 화합물을 제조하고 또 이 일반식(ⅩⅢ)의 화합물을 암모니아와 반응시키는 것을 포함하는 하기 일반식(Ⅲ) 화합물의 제조방법.
- 적당한 담채 및 / 또는 기타 보조제와 함께 활성 성분으로서 제1항 내지 제8항 또는 제10항에서 청구한 일반식(Ⅰ)또는 (Ⅱ) 화합물 또는 그의 염을 함유하는 농약 조성물.
- 동물 또는 식물에 있는 해충 및 아카리라(Acarina) 목(目의 대표적인 해충 방제용으로의 제1항 내지 제8항 또는 제10항에서 청구한 화합물 또는 그의 염의 용도.
- 제13항에 있어서, 유충단계의 식물 파괴 해충 방제용으로의 용도.
- 제13항에 있어서, 가축 및 생산성 가축의 외부기생체 방제용으로의 용도.
- 다양한 성장 단계에 있는 해충 또는 해충의 서식지를 제1항 내지 제8항 또는 제10항중 어느 하나에 따른 농약 활성 유효량 만큼의 일반식(Ⅰ)의 화합물 또는 그의 염, 또는 이러한 화합물을 적당한 보조제 및 담체와 함께 농약활성 유효량 만큼 함유하는 조성물로서 처리 또는 접촉시키는 것을 포함하는 해충 및 아카리나 목의 대표적인 해충의 방제 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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Application Number | Priority Date | Filing Date | Title |
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CH177286 | 1986-04-30 | ||
US01772/86-6 | 1986-04-30 |
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KR870010011A true KR870010011A (ko) | 1987-11-30 |
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KR870004197A KR870010011A (ko) | 1986-04-30 | 1987-04-30 | 치환된 2,4-디아미노-5-시아노 피리미딘 |
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US (1) | US4783468A (ko) |
EP (1) | EP0244360B1 (ko) |
JP (1) | JPH0688981B2 (ko) |
KR (1) | KR870010011A (ko) |
CN (1) | CN87103168A (ko) |
AR (1) | AR247389A1 (ko) |
AT (1) | ATE79614T1 (ko) |
AU (1) | AU598254B2 (ko) |
BR (1) | BR8702106A (ko) |
CA (1) | CA1292231C (ko) |
CS (1) | CS271471B2 (ko) |
DD (1) | DD270907A5 (ko) |
DE (1) | DE3781196D1 (ko) |
DK (3) | DK165690C (ko) |
ES (1) | ES2051771T3 (ko) |
GR (1) | GR3005856T3 (ko) |
HK (1) | HK11694A (ko) |
HU (3) | HU204396B (ko) |
IL (1) | IL82343A0 (ko) |
NZ (1) | NZ220132A (ko) |
PH (1) | PH24337A (ko) |
PT (1) | PT84774B (ko) |
SG (1) | SG135993G (ko) |
SU (2) | SU1657061A3 (ko) |
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US2941794A (en) * | 1956-04-13 | 1960-06-21 | Geddes Edith Bel | Building structures |
EP0508353B1 (de) * | 1991-04-11 | 1996-06-26 | Lonza Ag | Verfahren zur Herstellung von 4-Amino-2-chlor-5-cyan-6-(methylthio)pyrimidin |
RU95113597A (ru) * | 1992-12-02 | 1997-06-10 | ФМК Корпорейшн (US) | Инсектицидная композиция, способы борьбы с насекомыми |
US5344955A (en) * | 1993-02-19 | 1994-09-06 | Ciba-Geigy Corporation | Preparation of 1-amino-cyan-amido-2,2-dicyanoethylene, sodium salt |
DE4311901A1 (de) * | 1993-04-10 | 1994-10-13 | Huels Chemische Werke Ag | Neue Azeomethine, ein Verfahren zu ihrer Herstellung sowie deren Verwendung |
WO1995003282A2 (en) * | 1993-07-26 | 1995-02-02 | Ciba-Geigy Ag | Process for the preparation of substituted 4,6-diamino-5-cyanopyrimidines |
TR199802183T2 (en) * | 1996-04-29 | 2002-06-21 | Novartis Ag | B�cek �ld�r�c� bile�im. |
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AU2007202548B1 (en) * | 2007-06-01 | 2007-11-01 | Zoetis Services Llc | Pesticide Composition |
WO2009118312A1 (en) * | 2008-03-28 | 2009-10-01 | Novartis Ag | Dicyclanil formulation |
AU2010201828A1 (en) * | 2009-05-08 | 2010-11-25 | Jurox Pty Ltd | Veterinary composition |
WO2011035288A1 (en) | 2009-09-21 | 2011-03-24 | Merial Limited | Dicyclanil-based aqueous suspension and non-aqueous solution pour-on and spray on formulations for the prevention and treatment of insect infestation in animal |
CN102113496B (zh) * | 2010-01-03 | 2013-04-03 | 海利尔药业集团股份有限公司 | 一种含有环虫腈和灭多威的杀虫组合物 |
JP5731205B2 (ja) * | 2011-01-14 | 2015-06-10 | 株式会社エス・ディー・エス バイオテック | 農園芸用の有害生物防除剤としてのピリミジン誘導体 |
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CN102399193A (zh) * | 2011-12-15 | 2012-04-04 | 连云港市亚晖医药化工有限公司 | 4,6-二氨基-2-环丙胺基-5-腈基嘧啶的制备方法 |
CN103416420B (zh) * | 2012-05-18 | 2015-10-14 | 陕西汤普森生物科技有限公司 | 一种含环虫腈的杀虫组合物 |
CN103416430B (zh) * | 2012-05-24 | 2016-01-13 | 陕西汤普森生物科技有限公司 | 一种农药组合物 |
CN103444765A (zh) * | 2012-05-31 | 2013-12-18 | 陕西汤普森生物科技有限公司 | 一种含环虫腈与拟除虫菊酯类的杀虫组合物 |
JP2015003900A (ja) * | 2013-05-23 | 2015-01-08 | 宮崎みどり製薬株式会社 | ワクモ防除剤 |
CN103880759B (zh) * | 2014-01-28 | 2016-04-20 | 东南大学 | 一种地昔尼尔药物晶型ⅰ及其制备方法 |
CN104130197A (zh) * | 2014-07-29 | 2014-11-05 | 华中农业大学 | 2,4,6-三氨基-5-氰基嘧啶的化学合成方法 |
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- 1987-04-30 JP JP62107947A patent/JPH0688981B2/ja not_active Expired - Lifetime
- 1987-04-30 TR TR291/87A patent/TR22942A/xx unknown
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1988
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