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1. 发明申请

WO2006114405A2 USE OF 5-ALKYL-6-PHENYLALKYL-7-AMINO-AZOLOPYRIMIDINES, NOVEL AZOLOPYRIMIDINES, METHODS FOR THE PRODUCTION THEREOF, AND AGENTS CONTAINING THE SAME 审中-公开
标题翻译：使用5-烷基-6-苯基 - 7-氨基AZOLOPYRIMIDINEN，NEW azolopyrimidines，METHOD用于生产和AGENTS CONTAINING THE SAME
公开(公告)号：WO2006114405A2
公开(公告)日：2006-11-02
申请号：PCT/EP2006061786
申请日：2006-04-24
申请人： BASF AG , DIETZ JOCHEN , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , LOHMANN JAN KLAAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA
发明人： DIETZ JOCHEN , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , LOHMANN JAN KLAAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA
IPC分类号： A01N43/90
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to the use of 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidines of formula I for controlling phytopathogenic fungi. The variables in formula I have the following designations: Y represents alkylene, alkenylene or alkinylene, optionally substituted by alkyl groups; R 1 represents halogen, cyano, nitro, hydroxy, mercapto, alkyl, halogenalkyl, alkenyl, cycloalkyl, cycloalkenyl, alkoxy, halogenalkoxy, alkenyloxy, alkinyloxy, alkylthio, NR A R B , alkylcarbonyl, phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group O, N or S; R A , R B represent hydrogen, alkyl and alkylcarbonyl; n represents 0, 1, 2, 3 or 4; R 2 represents alkyl, alkenyl, cycloalkyl, alkoxyalkyl and alkylthioalkyl; R 3 represents hydrogen, halogen, cyano, NR A R B , hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phenylthio, benzyloxy, benzylthio, or alkyl-S(O) m- ; m represents 0, 1 or 2; A represents N and C-R a ; and R a represents hydrogen and alkyl. The carbon atoms in Y, R 1 , R 2 , R 3 and Ra can be substituted according to the description. The invention also relates to novel 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidines, to methods for producing said compounds, and to agents containing the same.
摘要翻译：式的5-烷基-6-苯基-7-氨基azolopyrimidinen的使用I：其中各变量具有以下含义：Y是任选被烷基取代的亚烷基，亚烯基或亚炔基; [R ^{1 为卤素，氰基，硝基，羟基，巯基，烷基，卤代烷基，链烯基，环烷基，环烯基，烷氧基，卤代烷氧基，烯氧基，炔氧基，烷硫基，NR ^{一 - [R < SUP>乙，烷基羰基，苯基，萘基或五 - 或六元饱和环，其包含选自一至四个杂原子的部分不饱和或罗马杂环O，N或S; [R ^{一，R ^{乙是氢，烷基和烷基羰基; n是零，1，2，3或4; [R ^{2 烷基，烯基，环烷基，烷氧基烷基和烷硫基烷基; [R ^{3 为氢，卤素，氰基，NR ^{一 - [R ^{乙，羟基，巯基，烷基，卤代烷基，环烷基，烷氧基，烷硫基，环烷氧基，环烷硫基，羧基，甲酰基，烷基羰基，烷氧基羰基，烯氧基羰基，炔氧基羰基，苯基，苯氧基，苯硫基，苄氧基，苄硫基，烷基-S（O）_{米 - ; m是0，1或2; A N和C-R ^{一; [R ^{一氢和烷基; 其中Y中的碳原子，R ^{1 ，R ^{2 ，R ^{3 和R a可以按照该描述被取代; 防治植物病原性有害真菌; 新5-烷基-6-苯基-7- aminoazolopyrimidines，处理用于制备这些化合物和含有它们的组合物。}}}}}}}}}}}}}}

2. 发明申请

WO2005087770A3 5,6-DIHYDROCARBYL-7-AMINO-TRIAZOLOPYRIMIDINES, METHOD FOR THEIR PRODUCTION, THEIR USE FOR CONTROLLING PATHOGENIC FUNGI AND AGENTS CONTAINING SAID COMPOUNDS 审中-公开
标题翻译： 5，6-二烃基 - 7-氨基三唑并嘧啶，其制造方法和它们用于防治有害真菌和代理含
公开(公告)号：WO2005087770A3
公开(公告)日：2005-12-08
申请号：PCT/EP2005002424
申请日：2005-03-08
申请人： BASF AG , TORMO I BLASCO JORDI , BLETTNER CARSTEN , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , NIEDENBRUECK MATTHIAS , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD , HUENGER UDO
发明人： TORMO I BLASCO JORDI , BLETTNER CARSTEN , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , NIEDENBRUECK MATTHIAS , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD , HUENGER UDO
IPC分类号： C07D487/04
CPC分类号： C07D487/04
摘要： The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R represents alkyl, alkoxyalkyl, alkenyl or alkynyl; R represents alkyl, alkoxyalkyl, alkenyl or alkynyl, R and/or R being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
摘要翻译： 5,6-二烷基 - 7-氨基三唑并嘧啶，其中取代基具有式（I）的以下含义：R t <1>是烷基，烷氧基烷基，烯基或炔基; [R <2>是烷基，烷氧基烷基，烯基或炔基; 其中R <1>和/或R <2>取代根据描述; 一种用于制备这些化合物，含有它们和它们在防治植物病原性有害真菌的用途的组合物的过程。

3. 发明申请

WO2005121146A3 1, 2, 4-TRIAZOLO[1,5A]PYRIMIDINES AND USE THEREOF FOR CONTROLLING PLANT-PATHOGENIC FUNGI 审中-公开
标题翻译： 1，2，4-三唑并[1,5-α]嘧啶和它们用于防治植物病原真菌
公开(公告)号：WO2005121146A3
公开(公告)日：2006-02-16
申请号：PCT/EP2005006171
申请日：2005-06-08
申请人： BASF AG , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
发明人： BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
IPC分类号： C07D487/04 , A01N43/647 , A01N43/90 , C07D487/00
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to triazolopyrimidines of formula (I), wherein the index n and the substituents R, R
摘要翻译：本发明涉及下式的三唑并嘧啶I，其中索引n和取代基R，R

4. 发明申请

WO2006092428A2 2-SUBSTITUTED 7-AMINO-AZOLOPYRIMIDINE, A METHOD FOR THE PRODUCTION AND USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI AND AGENTS CONTAINING SAID COMPOUND 审中-公开
标题翻译： 2-取代的7- aminoazolopyrimidines，METHOD用于生产和它们用于防治有害真菌和代理含
公开(公告)号：WO2006092428A2
公开(公告)日：2006-09-08
申请号：PCT/EP2006060399
申请日：2006-03-02
申请人： BASF AG , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , LOHMANN JAN KLAAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHWOEGLER ANJA , RACK MICHAEL
发明人： GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , LOHMANN JAN KLAAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHWOEGLER ANJA , RACK MICHAEL
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： C07D487/04
摘要： The invention relates to 2-substituted 7-amino-azolopyrimidine of formula (I), wherein substituents have the following meanings: R 1 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, Cycloalkyl, alkoxy, alkoxyalkyl, benzyloxyalkyl, alkoxyalkenyl or akoxyalkinyl; R 2 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkoxyalkyl and alkylthioalkyl, wherein a carbon chain in R 1 and/or R 2 are substitutable according to a description; R 3 is halogen, Cyano, NR A R B , hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phe- nylthio, benzyloxy, benzylthio, alkyl-S(O) m- ; A N and CR x ; R x is hydrogen or one of above groups for R 3 . A method and intermediate products for producing said compounds, agents containing said compounds and the use thereof for combating plant-pathogen fungi are also disclosed.
摘要翻译： 2-取代的式（I）其中取代基具有以下含义的7-氨基azolopyrimidines：R t ^{1 为氢，卤素，氰基，烷基，卤代烷基，烯基，炔基，环烷基，烷氧基，烷氧基烷基， benzyloxyalkyl，烷氧基烯基或alkoxyalkynyl; [R ^{2 为氢，卤素，氰基，烷基，卤代烷基，烯基，炔基，环烷基，烷氧基，烷氧基烷基和烷硫基烷基，其中在R中的碳链^{1 和/或R ^{2 可以根据描述被取代; [R ^{3 为卤素，氰基，NR ^{一 - [R ^{乙，羟基，巯基，烷基，卤代烷基，环烷基，烷氧基，烷硫基，环烷氧基，环烷硫基，羧基，甲酰基，烷基羰基，烷氧基羰基，烯氧基羰基，炔氧基羰基，苯基，苯氧基，苯丙氨酸nylthio，苄氧基，苄硫基，烷基-S（O）_{米 - ; A N和CR ^{X ; ，R 3 基^{X 是氢或其中R ^{称作; 的方法和中间体制备这些化合物，含有它们和它们在防治植物病原性有害真菌的组合物。}}}}}}}}}}}

5. 发明申请

WO2005095404A3 6-(2-FLUOROPHENYL)-TRIAZOLOPYRIMIDINES, METHOD FOR PRODUCING THEM, THEIR USE FOR CONTROLLING PARASITIC FUNGI AND AGENTS CONTAINING THE SAME 审中-公开
标题翻译： 6-（2-氟苯基） - 三唑并嘧啶，防治有害真菌和代理CONTAINING生产和使用方法
公开(公告)号：WO2005095404A3
公开(公告)日：2006-04-06
申请号：PCT/EP2005003208
申请日：2005-03-26
申请人： BASF AG , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
发明人： BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
IPC分类号： C07D487/04 , A01N43/90
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to the 6-(2-fluorophenyl)-triazolopyrimidines of formula (I), wherein the substituents are defined as follows: R
摘要翻译：本申请公开了式-6-（2-氟苯基） - 三唑并嘧啶予其中的取代基具有下列含义：R t

6. 发明申请

WO2005095405A3 6-(2,6-DICHLOROPHENYL)-TRIAZOLOPYRIMIDINES, METHODS FOR THE PRODUCTION THEREOF, USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI, AND AGENTS CONTAINING THE SAME 审中-公开
标题翻译： 6-（2,6-二氯 - 苯基） - 三唑并嘧啶，防治有害真菌和代理CONTAINING生产和使用方法
公开(公告)号：WO2005095405A3
公开(公告)日：2005-12-22
申请号：PCT/EP2005004187
申请日：2005-03-29
申请人： BASF AG , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
发明人： BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , RACK MICHAEL , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
IPC分类号： A01N43/90 , C07D487/04
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R and R can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R and R together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.
摘要翻译： 6-（2,6-二氯苯基） - 三唑并嘧啶的式（I）的其中取代基具有以下含义：R t <1>，R <2>是氢，烷基，卤代烷基，环烷基，卤代环烷基，烯基，卤代烯基，环烯基，卤代环烯基基，炔基，卤代炔基，或苯基，萘基，或含有选自O，N，或S，R <1>和R <2>也可以，一起一至四个杂原子的五元或六元饱和，部分不饱和或芳族杂环形成一个五元或六元杂环基或杂芳基的氮原子与它们所连接，这是经N个附接和选自O，N和S的一至三个另外的杂原子作为环成员，并且可以根据该描述被取代; X为烷基，氰基，烷氧基，卤代烷氧基，烯氧基或卤代链烯氧基，其中X不为C1-C4烷基，当R <1>和R <2>是常见的哌啶-1-基或4-甲基 - 哌啶-1-基; 一种用于制备这些化合物，含有它们和它们在防治植物病原性有害真菌的用途的组合物的过程。

7. 发明申请

WO2005110080A2 FUNGICIDAL MIXTURES AND NOVEL TRIAZOLOPYRIMIDINES 审中-公开
标题翻译：杀真菌剂混合物及新三唑
公开(公告)号：WO2005110080A2
公开(公告)日：2005-11-24
申请号：PCT/EP2005005070
申请日：2005-05-11
申请人： BASF AG , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
发明人： BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , HUENGER UDO , MUELLER BERND , NIEDENBRUECK MATTHIAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , WAGNER OLIVER , NAVE BARBARA , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH , STIERL REINHARD
IPC分类号： A01N20060101 , A01N43/90 , A01N
CPC分类号： A01N43/90 , A01N59/06 , A01N59/02 , A01N57/12 , A01N47/38 , A01N47/34 , A01N47/24 , A01N47/04 , A01N43/50 , A01N43/76 , A01N43/653 , A01N43/36 , A01N43/40 , A01N43/32 , A01N37/48 , A01N37/46 , A01N37/38 , A01N37/34 , A01N2300/00
摘要： The invention relates to fungicidal mixtures containing in the form of active components 1) 5-methyl-7-amino-triazolopyrimidine of formula (I), wherein R is alkyl, halogenalkyl, alkenyl or cyclopentyl, R is hydrogen or alkyl, R and R together with the nitrogen atom to which they are bound may form a piperidinyl cycle substitutable by a methyl group, L is fluorine or chlorine, L , L are independently from each other hydrogen, fluorine or chlorine and 2) at least one type of active substance selected from groups A) azoles, B) strobilurins, C) acyl alanines, D) amine derivatives, E) anilinopyrimidines; F) dicarboximides; G) cinnamic acid amides and analogues thereof, H) antibiotics, K) dithiocarbamates, L) heterocyclic compounds, M) sulphur and copper fungicides, N) nitrophenyl derivatives, O) phenylpyrroles, P) sulfenic acid derivatives, Q) other fungicides and R) growth retardants according to the descriptions, wherein said mixtures contain the compounds in a synergically efficient amount. Novel triazolopyrimidines, methods for controlling pathogenic fungi using the mixtures of the compound (I) with active substances of the groups A) and R), the use the compounds (I) with the active substances of the groups A) and R) for producing said mixtures and agents containing said mixtures are also disclosed.
摘要翻译：一种杀真菌混合物，其包含作为活性组分：1）式（I）的5-甲基-7-氨基三唑并嘧啶，其中R <1>是烷基，卤代烷基，链烯基或环戊基; [R <2>是氢或烷基; [R <1>和R <2>也可以与氮原子一起与它们所连接的形式，其可以由甲基取代的哌啶环; →<1>是氟或氯; →<2>，L <3>独立地是氢，氟或氯; 和2）选自组A）唑类中的至少一种活性化合物; B）嗜球果伞素; C）酰基丙氨酸类; D）胺衍生物; E）苯胺基嘧啶; F）二甲酰亚胺; G）肉桂酸和类似物; 1H）抗生素; K）二硫代氨基甲酸酯; L）杂环化合物; M）硫和铜杀真菌剂; N）硝基苯基衍生物; O）苯基吡咯; P）Sulfensäurederivate; Q）其他杀菌剂; R）Wachstumsretardantien; 根据描述; 在协同有效量; 新的三唑并嘧啶，用于控制使用I化合物的混合物与基团A），以R的活性成分）包含这些混合物的有害真菌及其制造这样的混合物使用I化合物与基团A）至R）的活性成分和组合物的方法，

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