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1. 发明申请

WO2005010000A3 ARYL-CONDENSED 3-ARYLPYRIDINE COMPOUNDS AND USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI 审中-公开
标题翻译：芳基稠合的3-芳基吡啶化合物及其用于控制破损蘑菇的用途
公开(公告)号：WO2005010000A3
公开(公告)日：2005-05-19
申请号：PCT/EP2004007924
申请日：2004-07-15
申请人： BASF AG , WAGNER OLIVER , GROTE THOMAS , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GYPSER ANDREAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , TORMO I BLASCO JORDI , AKERS ALAN , SPEAKMAN JOHN-BRYAN , RACK MICHAEL , STIERL REINHARD , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH
发明人： WAGNER OLIVER , GROTE THOMAS , BLETTNER CARSTEN , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GYPSER ANDREAS , MUELLER BERND , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , TORMO I BLASCO JORDI , AKERS ALAN , SPEAKMAN JOHN-BRYAN , RACK MICHAEL , STIERL REINHARD , SCHERER MARIA , STRATHMANN SIEGFRIED , SCHOEFL ULRICH
IPC分类号： A01N43/90 , C07D471/04
CPC分类号： C07D471/04 , A01N43/90
摘要： The invention relates to bicyclic compounds of general formula I, wherein X, Y independently represent N or C-R ; n stands for 1, 2, 3, 4 or 5; R represents halogen, cyano, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-halogenalkyl, C1-C6-halogenalkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy or C(O)R ; R denotes halogen, cyano, C1-C6-alkyl, C1-C6-halogenalkyl, C2-C6-alkenyl, C2-C6-alkinyl, C3-C8-cycloalkyl, optionally mono- or polysubstituted by alkyl and/or halogen, C5-C8 cycloalkenyl, optionally mono- or polysubstituted by alkyl and/or halogen, OR , SR or NR R ; R denotes halogen, cyano, C1-C6-alkyl, C1-C6-halogenalkyl, C2-C6-alkenyl, C2-C6-alkinyl, C3-C8-cycloalkyl, optionally mono- or polysubstituted by alkyl and/or halogen, C5-C8-cycloalkenyl, optionally mono- or polysubstituted by alkyl and/or halogen, OR , SR or NR R , and R represents hydrogen, C1-C6-alkyl, C1-C6-halogenalkyl or C3-C6-cycloalkyl, optionally mono- or polysubstituted by alkyl and/or halogen. Said invention also relates to the agriculturally-acceptable salts of said compounds (I), plant protection agents, containing at least one compound of general formula (I) and/or one agriculturally-acceptable salt of (I) and at least one liquid or solid carrier substance, as well as a method for controlling phytopathogenic fungi.
摘要翻译：本发明涉及通式I的双环化合物，其中X，Y彼此独立地是N或C-R 4; n是1,2,3,4或5; ř表示卤素，氰基，C1-C6烷基，C1-C6烷氧基，C1-C6卤代烷基，C1-C6卤代烷氧基，C2-C6链烯基，C2-C6链烯氧基或C （O）R 5代表; [R <1>为卤素，氰基，C1-C6烷基，C1-C6卤代烷基，C2-C6链烯基，C2-C6炔基，C3-C8-环烷基，其任选被烷基和/或卤素取代的或者多取代，C5-C8环烯基，其任选与乘法烷基和/或卤素或单 - ，或<6>，SR <6>或NR <7> - [R <8>取代; [R <2>为卤素，氰基，C1-C6烷基，C1-C6卤代烷基，C2-C6链烯基，C2-C6炔基，C3-C8环烷基，任选地被烷基和/或卤素单取代的或多取代的，C5-C8环烯基，其任选地被烷基和/或卤素取代基取代一次或多次，或<6>，SR <6>或NR <7> - [R <8>; R 3是任选被烷基和/或卤素单取代或多取代的氢，C 1 -C 6烷基，C 1 -C 6卤代烷基或C 3 -C 6环烷基; 和化合物（I），植物保护剂的农业上可接受的盐，其包含通式（I）和/或（I）的农业上可接受的盐和至少一种液体或固体载体和用于防治植物病原性有害真菌的方法中的至少一种化合物。

2. 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

3. 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。

4. 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

5. 发明申请

WO03008417A9 SUBSTITUTED 6-(2-TOLYL)-TRIAZOLOPYRIMIDINES AS FUNGICIDES 审中-公开
标题翻译：取代的6-（2-甲苯基） - 三唑并嘧啶作为杀真菌剂
公开(公告)号：WO03008417A9
公开(公告)日：2003-10-30
申请号：PCT/EP0207578
申请日：2002-07-08
申请人： BASF AG , TORMO I BLASCO JORDI , SAUTER HUBERT , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
发明人： TORMO I BLASCO JORDI , SAUTER HUBERT , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC分类号： A01N43/90 , C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R and R independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R and R radicals may be unsubstituted or substituted as defined in the description, or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
摘要翻译：式（I）的取代的6-（2-甲苯基） - 三唑并嘧啶，其中R 1和R 2独立地表示氢或烷基，烯基，炔基或链二烯基，卤代烷基，卤代烯基，环烷基，苯基，萘基或含有1至4个氮原子或1至3个氮原子和1个硫或氧原子的5-或6-元杂环基，或者含有1-4个氮原子或1-3个氮原子的5-或6-元杂芳基，硫或氧原子，或者其中R 1和R 2基团可以如说明书中所定义的那样未被取代或被取代，或者R 1和R 2与中间的氮原子一起表示5或6 - 含有1至4个氮原子或1至3个氮原子和1个硫或氧原子的可被取代的 - 元杂环; R 3是卤素，氰基，烷基，烷氧基，卤代烷基或C（= O）A，其中A是氢，羟基，烷基，氨基或单或二烷基氨基; n是1至4的整数; X是卤素，氰基，烷基，烷氧基，卤代烷氧基或烯氧基; 它们的制备方法，含有它们的组合物以及它们用于防治植物病原性真菌的用途。

6. 发明申请

WO03004465A2 FUNGICIDAL TRIAZOLOPYRIMIDINES, METHOD FOR THE PRODUCTION THEREOF AND USE THEREOF IN CONTROLLING NOXIOUS FUNGI AND AGENTS CONTAINING SAID COMPOUNDS 审中-公开
标题翻译：三唑杀真菌剂，制造方法及其用于防治有害真菌剂含
公开(公告)号：WO03004465A2
公开(公告)日：2003-01-16
申请号：PCT/EP0207340
申请日：2002-07-03
申请人： BASF AG , MUELLER BERND , SAUTER HUBERT , GEWEHR MARKUS , GRAMMENOS WASSILIOS , TORMO I BLASCO JORDI , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , LORENZ GISELA , STRATHMANN SIEGFRIED , AMMERMANN EBERHARD , STIERL REINHARD
发明人： MUELLER BERND , SAUTER HUBERT , GEWEHR MARKUS , GRAMMENOS WASSILIOS , TORMO I BLASCO JORDI , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , LORENZ GISELA , STRATHMANN SIEGFRIED , AMMERMANN EBERHARD , STIERL REINHARD
IPC分类号： A01N43/90 , C07D487/04 , C07D , A01N , C07C
CPC分类号： C07D487/04 , A01N43/90
摘要： Triazolopyrimidines of formula (I), wherein the index and substituents have the following meaning: n = 0 or a whole number of 1 - 5; R = halogen, cyano, hydroxy, cyanate, alkyl, alkenyl, alkinyl, halogenalkyl, halogenalkenyl, alkoxy, alkenyloxy, alkinyloxy, halogenalkoxy, cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkinyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl, cycloalkylcarbonyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S; R = alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, phenyl, naphthyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S, R and/or R being able to be substituted according to the description; R = alkyl, alkenyl or alkinyl which can be substituted by halogen, cyano, nitro, alkoxy or alkoxycarbonyl. The invention also relates to a method for the production of said compounds, agents containing same, and the use thereof in controlling noxious fungi.
摘要翻译：式（I），其中所述索引和所述取代基具有以下含义的三唑并嘧啶：n是0或1〜5的整数; R是卤素，氰基，羟基，氰酸酯，烷基，烯基，炔基，卤代烷基，卤代烯基，烷氧基，链烯氧基，炔氧基，卤代烷氧基，环烷基，环烯基，环烷氧基，烷氧基羰基，烯氧基羰基，炔氧基羰基，氨基羰基，烷基氨基羰基，二烷基氨基羰，alkoximinoalkyl，Alkenyloximinocarbonyl，Alkinyloximinoalkyl 羰基，烯基，炔基羰基，环烷基羰基，或5至10元的饱和，其包含选自一至四个杂原子的部分不饱和或芳族杂环O，N或S; [R <1>是烷基，烯基，炔基，环烷基，环烯基，苯基，萘基，或5至10元饱和，部分不饱和或芳族，其包含从O型一至四个杂原子的杂环，N或S，其中R和/ 或者R 1可以如上所述被取代; [R <2>是烷基，烯基或炔基，可被卤素，氰基，硝基，烷氧基或烷氧羰基取代; 一种用于制备这些化合物，含有它们以及它们在防治有害真菌中的用途的组合物的过程。

7. 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。}}}}}}}}}}}

8. 发明申请

WO9920615A3 PESTICIDE SUBSTITUTED PHENYL CARBAMATES, METHODS AND INTERMEDIATE PRODUCTS FOR PRODUCING THEM, AND USE OF THE SAME 审中-公开
标题翻译：杀虫剂取代的苯基氨基甲酸酯，其制备方法和中间体产品及其使用
公开(公告)号：WO9920615A3
公开(公告)日：1999-06-24
申请号：PCT/EP9806299
申请日：1998-10-05
申请人： BASF AG , BAYER HERBERT , GEWEHR MARKUS , GROTE THOMAS , MUELLER BERND , SAUTER HUBERT , GRAMMENOS WASSILIOS , GYPSER ANDREAS , PTOCK ARNE , GOETZ ROLAND , RACK MICHAEL , ROEHL FRANZ , AMMERMANN EBERHARD , HARRIES VOLKER , LORENZ GISELA , STRATHMANN SIEGFRIED
发明人： BAYER HERBERT , GEWEHR MARKUS , GROTE THOMAS , MUELLER BERND , SAUTER HUBERT , GRAMMENOS WASSILIOS , GYPSER ANDREAS , PTOCK ARNE , GOETZ ROLAND , RACK MICHAEL , ROEHL FRANZ , AMMERMANN EBERHARD , HARRIES VOLKER , LORENZ GISELA , STRATHMANN SIEGFRIED
IPC分类号： A01N43/82 , A01N43/836 , C07C259/14 , C07C265/12 , C07D271/06 , C07D271/07 , C07D413/12 , C07C239/12 , C07C251/38 , C07D413/14
CPC分类号： C07D271/07 , A01N43/82 , C07C259/14 , C07C265/12 , C07D413/12
摘要： The invention relates to substituted phenyl carbamates of formula (I), wherein E represents a group A or B, # characterises the bond with the phenyl ring, and R , R , Y, n, T, and Z have the meanings given in the description.
摘要翻译：本发明涉及式（I），其中E是基团A或B，其中＃为键合到苯基环的特征的取代的苯基氨基甲酸酯，且R <阿尔法>，R <克（B）>，Y，N，T 和Z具有描述中给出的含义。

9. 发明申请

WO03090539A8 3-HETEROARYL SUBSTITUTED 5-METHYLOXYMETHYL ISOXAZOLINES USED AS HERBICIDES 审中-公开
标题翻译： 3 - 杂芳基 - 取代的异恶唑啉5甲氧基甲基-AS除草剂
公开(公告)号：WO03090539A8
公开(公告)日：2004-12-16
申请号：PCT/EP0304136
申请日：2003-04-22
申请人： BASF AG , WAGNER OLIVER , RACK MICHAEL , WITSCHEL MATTHIAS , ZAGAR CYRILL , LANDES ANDREAS
发明人： WAGNER OLIVER , RACK MICHAEL , WITSCHEL MATTHIAS , ZAGAR CYRILL , LANDES ANDREAS
IPC分类号： A01N43/80 , C07D261/08 , C07D413/04 , C07D413/14 , C07D417/04
CPC分类号： C07D413/04 , A01N43/80 , C07D261/08 , C07D413/14 , C07D417/04
摘要： The invention relates to 3-heteroaryl substituted isoxazolines of formula (I), or to their salts that can be used for agricultural purposes. In said formula, the variables are defined as follows: X represents a substituted 5-membered heteroaryl comprising between one and four nitrogen atoms, or between one and three nitrogen atoms and one oxygen or sulphur atom, or one oxygen or sulphur atom, or represents a substituted 6-membered heteroaryl comprising between one and four nitrogen atoms, whereby the aforementioned 5-membered heteroaryl is not pyrazolyl or thienyl; R - R represent hydrogen, alkyl or haloalkyl; Y represents an optionally substituted aryl, or benzo[1,4]dioxonyl, benzo[1,3]dioxolanyl, 2,3-dihydrobenzofuranyl or benzimidazole, or an optionally substituted 5- to 6-membered heteroaryl. The invention also relates to methods and intermediate products for the production of said compounds, in addition to the use thereof or of agents containing the compounds for controlling undesired plants.
摘要翻译：本发明涉及式（I）的3- heteroarylsubstituerte异恶唑啉：其中各变量具有以下含义：X为取代的具有一至四个氮原子或具有一至三个氮原子和一个氧或硫原子，或具有5元杂芳基一个氧或硫原子; 的或取代的具有一至四个氮原子的6元杂芳基; 其中，上述的5元杂芳基未被吡唑基或噻吩基; [R <1> - R的<7>是氢，烷基或卤代烷基; Y是任选取代的芳基，或苯并[1,4] dioxonyl，苯并[1,3]二氧戊环基，2,3-二氢苯并呋喃基或苯并咪唑; 或任选取代的5-至6-元杂芳基; 及其可农用盐，它们的制备方法和中间体; 和使用这些化合物或包含用于控制不希望的植物的装置这些化合物。

10. 发明申请

WO2008152138A3 METHOD FOR PRODUCING DIFLUOROMETHYL-SUBSTITUTED PYRAZOLE COMPOUNDS 审中-公开
标题翻译：用于生产二氟吡唑
公开(公告)号：WO2008152138A3
公开(公告)日：2009-05-28
申请号：PCT/EP2008057506
申请日：2008-06-13
申请人： BASF SE , NETT MARKUS , GROTE THOMAS , LOHMANN JAN KLAAS , DIETZ JOCHEN , SMIDT SEBASTIAN PEER , RACK MICHAEL , ZIERKE THOMAS
发明人： NETT MARKUS , GROTE THOMAS , LOHMANN JAN KLAAS , DIETZ JOCHEN , SMIDT SEBASTIAN PEER , RACK MICHAEL , ZIERKE THOMAS
IPC分类号： C07D231/12 , C07D231/14
CPC分类号： C07D231/12 , C07D231/14
摘要： The invention relates to a method for producing 3-difluoromethyl-substituted pyrazole compounds of formula (I), wherein R1 represents H, halogen, nitro, C1-C8 alkyl, C1-C8 haloalkyl, C3-C8 cycloalkyl, phenyl, naphthyl, hetaryl, cyano, -C(=O)-OR1a, -C(=O)-NR1bR1c, -C(=O)-SR1d or -C(=S)-SR1 e; R2 represents H, C1-C4 alkyl, benzyl or phenyl; R3 represents H, halogen, C1-C8 alkoxy, C1-C8 haloalkoxy, C3-C8 cycloalkoxy, C2-C8 alkenyloxy, C1-C8 alkylthio, C1-C8 haloalkylthio, C3-C8 cycloalkylthio or C2-C8 alkenylthio; to compounds of formula (II.a) or (II.b), wherein R1 and R3 have one of the above definitions; R4 represents halogen, -OR4a, -SR4a , -O-SO2-R4a or a group -NR4bR4c; R5 and R6 represent C1-C8 alkyl, C1-C8 haloalkyl, C3-C8 cycloalkyl, benzyl or phenyl or together with the nitrogen atom to which they are bound represent a 3- to 8-membered heterocycle; to Lewis acid adducts of compounds of formula (II.b); to the use of compounds of formula (II.a) or (II.b) and of the Lewis acid adducts thereof for producing compounds of formula (I) or (VI); and to a method for converting said compounds to the corresponding 3-difluoromethylpyrazole-4-yl carboxylic acids.
摘要翻译：本发明涉及一种用于制备式-3-二氟甲基吡唑（I）化合物其中R1是H，卤素，硝基，C1-C8烷基，C1-C8卤代烷基，C3-C8环烷基，苯基，萘基，杂芳基，氰基，-C（= O）-OR1a，-C（= O）-NR1bR1c，-C（= O）-SR1d或-C（= S）-SR1e基; R2是H，C1-C4烷基，苄基或苯基; R 3为H，卤素，C1-C8烷氧基，C1-C8卤代烷氧基，C3-C8环烷氧基，C2-C8链烯氧基，C1-C8烷硫基，C1-C8卤代烷硫基，C3-C8-环烷硫基或C 2 -C C8-烯硫基;式（二.a）或（二.b）的化合物，其中R 1和R 3具有以上给出的含义之一; R 4是卤素，-OR4a，-SR4a，-O-SO2-R4A或一组-NR4bR4c基; R5和R6是C1-C8烷基，C1-C8卤代烷基，C3-C8环烷基，苄基或苯基或一起与氮原子到它们所键合的，代表3-至8-元杂环; 式（二.b）化合物的路易斯酸加合物;使用（二.a）或（二.b）和路易斯酸加合物，式I化合物的对式（I）或（VI）的化合物的制备方法; 并且这些化合物转变成相应的3-二氟甲基吡唑-4-基甲磺酸的方法。

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