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1. 发明授权

EP0550113B1 Triazolopyrimidine derivatives with fungicidal activity 失效
标题翻译：用的杀真菌活性的三唑并嘧啶衍生物
公开(公告)号：EP0550113B1
公开(公告)日：1997-10-15
申请号：EP92204097.7
申请日：1992-12-28
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Pees, Klaus-Jürgen , Albert, Guido
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90

2. 发明授权

EP0613900B1 Triazolopyrimidine derivatives with fungicidal activity 失效
标题翻译：用的杀真菌活性的三唑并嘧啶衍生物
公开(公告)号：EP0613900B1
公开(公告)日：1997-05-14
申请号：EP94200532.3
申请日：1994-03-02
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Pees, Klaus-Jürgen
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90

3. 发明公开

EP0550113A2 Triazolopyrimidine derivatives with fungicidal activity 失效
标题翻译： Triazolopyrimidinderivate mit fungiziderAktivität。
公开(公告)号：EP0550113A2
公开(公告)日：1993-07-07
申请号：EP92204097.7
申请日：1992-12-28
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Pees, Klaus-Jürgen , Albert, Guido
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90
摘要： This invention relates to certain triazolopyrimidine derivatives of the general formula

in which R¹ represents an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, cycloalkyl, bicycloalkyl or heterocyclyl group; R² represents a hydrogen atom or an alkyl group; or R¹ and R² together with the interjacent nitrogen atom represent an optionally substituted heterocyclic ring; R³ represents an optionally substituted aryl group; and R⁴ represents a hydrogen or halogen atom or a group -NR⁵R⁶ where R⁵ represents a hydrogen atom or an amino, alkyl, cycloalkyl or bicycloalkyl group and R⁶ represents a hydrogen atom or an alkyl group; processes for their preparation; compositions containing such compounds and their use as fungicides.
摘要翻译：本发明涉及某些通式“CHEM”的三唑并嘧啶衍生物，其中R 1表示任选取代的烷基，烯基，炔基，链二烯基，环烷基，双环烷基或杂环基; R 2表示氢原子或烷基; 或R 1和R 2与所述中间氮原子一起表示任选取代的杂环; R 3表示任选取代的芳基; 并且R 4表示氢或卤素原子或基团-NR 5 R 6，其中R 5表示氢原子或氨基，烷基，环烷基或双环烷基，R 6表示氢原子或烷基; 其准备过程; 含有这些化合物的组合物及其作为杀真菌剂的用途。

4. 发明公开

EP0613900A1 Triazolopyrimidine derivatives with fungicidal activity 失效
标题翻译： Triazolopyrimidinderivate mit fungiziderAktivität。
公开(公告)号：EP0613900A1
公开(公告)日：1994-09-07
申请号：EP94200532.3
申请日：1994-03-02
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Pees, Klaus-Jürgen
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90
摘要： This invention relates to certain triazolopyrimidine derivatives of the general formula

in which R¹ represents an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, cycloalkyl, bicycloalkyl or heterocyclyl group; R² represents a hydrogen atom or an alkyl group; or R¹ and R² together with the interjacent nitrogen atom represent an optionally substituted cycloalkyl or heterocyclic ring; R³ represents an optionally substituted cycloalkyl or heterocyclyl group; and R⁴ represents a hydrogen or halogen atom or a group -NR⁵R⁶ where R⁵ represents a hydrogen atom or an amino, alkyl, cycloalkyl or bicycloalkyl group and R⁶ represents a hydrogen atom or an alkyl group; processes for their preparation; compositions containing such compounds and their use as fungicides.
摘要翻译：本发明涉及某些通式“CHEM”的三唑并嘧啶衍生物，其中R 1表示任选取代的烷基，烯基，炔基，链二烯基，环烷基，双环烷基或杂环基; R 2表示氢原子或烷基; 或R 1和R 2与中间的氮原子一起表示任选取代的环烷基或杂环; R 3表示任选取代的环烷基或杂环基; 并且R 4表示氢或卤素原子或基团-NR 5 R 6，其中R 5表示氢原子或氨基，烷基，环烷基或双环烷基，R 6表示氢原子或烷基; 其准备过程; 含有这些化合物的组合物及其作为杀真菌剂的用途。

5. 发明公开

EP0550113A3 Triazolopyrimidine derivatives with fungicidal activity 失效
标题翻译：具有杀真菌活性的三唑基嘧啶衍生物
公开(公告)号：EP0550113A3
公开(公告)日：1993-08-04
申请号：EP92204097.7
申请日：1992-12-28
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Pees, Klaus-Jürgen , Albert, Guido
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90
摘要： This invention relates to certain triazolopyrimidine derivatives of the general formula

in which R¹ represents an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, cycloalkyl, bicycloalkyl or heterocyclyl group; R² represents a hydrogen atom or an alkyl group; or R¹ and R² together with the interjacent nitrogen atom represent an optionally substituted heterocyclic ring; R³ represents an optionally substituted aryl group; and R⁴ represents a hydrogen or halogen atom or a group -NR⁵R⁶ where R⁵ represents a hydrogen atom or an amino, alkyl, cycloalkyl or bicycloalkyl group and R⁶ represents a hydrogen atom or an alkyl group; processes for their preparation; compositions containing such compounds and their use as fungicides.

6. 发明公开

EP0491441A1 Fungicidal isoquinoline derivatives 失效
标题翻译： Fungizide Isochinolinderivate。
公开(公告)号：EP0491441A1
公开(公告)日：1992-06-24
申请号：EP91203316.4
申请日：1991-12-16
申请人： SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V.
发明人： Bissinger, Hans-Joachim , Schröder, Ludwig , Albert, Guido , Pees, Klaus-Jürgen
IPC分类号： C07D217/16 , C07D217/22 , A01N43/42 , C07D217/14 , C07D491/04
CPC分类号： C07D401/10 , A01N43/42 , A01N43/90 , C07D217/02 , C07D217/14 , C07D217/16 , C07D217/22 , C07D491/04
摘要： The invention provides a method of combating fungus at a locus which comprises treating the locus with a compound of the general formula

or an N-alkyl or N-phenyl halide or N-oxide thereof, in which R¹, R², R³ and R⁴ independently represent a hydrogen or halogen atom, a hydroxyl group or an optionally substituted alkyl or alkoxy group, or R¹ and R² or R² and R³ or R³ and R⁴ together with the interjacent carbon atoms represent a 5- to 7-membered saturated or unsaturated carbocyclic or heterocyclic ring in which a heterocyclic ring contains 1 to 3 heteroatoms selected from nitrogen, oxygen and sulphur atoms; R⁵ represents a hydrogen or halogen atom, R⁶ represents a hydrogen atom, or R⁵ and R⁶ together represent a single carbon- carbon bond; R⁷ represents a hydrogen or halogen atom, an alkyl or alkoxy group optionally substituted by one or more halogen atoms, or an optionally substituted phenyl or phenoxy group; R⁸ and R⁹ independently represent a hydrogen atom or together represent a single carbon-carbon bond; and A represents an optionally substituted phenyl group. Certain of the isoquinoline derivatives are novel and a process for the preparation of these compounds and compositions containing them are also provided.
摘要翻译：本发明提供了一种抗病原菌的方法，该方法包括用通式为CHEM的化合物或N-烷基或N-苯基卤化物或其N-氧化物处理所述场所，其中R 1，R R 3和R 4独立地表示氢或卤素原子，羟基或任意取代的烷基或烷氧基，或R 1和R 2或R 2和R 3或R 3和R 4与中间碳原子一起代表5-至7-元饱和或不饱和的碳环或杂环，其中杂环含有1-3个选自氮，氧和硫原子; R 5表示氢或卤素原子，R 6表示氢原子，或R 5和R 6共同表示单个碳 - 碳键; R 7表示氢或卤素原子，任选被一个或多个卤素原子取代的烷基或烷氧基，或任选取代的苯基或苯氧基; R 8和R 9独立地表示氢原子或一起代表单个碳 - 碳键; 并且A表示任选取代的苯基。某些异喹啉衍生物是新颖的，还提供了制备这些化合物的方法和含有它们的组合物。

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