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11. 发明授权

US07501530B2 Trifluoromethyl-thiophene carboxylic acid aniledes and use thereof as fungicides 失效
标题翻译：三氟甲基 - 噻吩羧酸和其作为杀真菌剂的用途
公开(公告)号：US07501530B2
公开(公告)日：2009-03-10
申请号：US10548840
申请日：2004-03-20
申请人： Markus Gewehr , Bernd Müller , Thomas Grote , Wassilios Grammenos , Andreas Gypser , Jordi Tormo i Blasco , Anja Schwögler , Joachim Rheinheimer , Carsten Blettner , Frank Schieweck , Michael Rack , Ulrich Schöfl , Siegfried Strathmann , Reinhard Stierl , Jan Rether
发明人： Markus Gewehr , Bernd Müller , Thomas Grote , Wassilios Grammenos , Andreas Gypser , Jordi Tormo i Blasco , Anja Schwögler , Joachim Rheinheimer , Carsten Blettner , Frank Schieweck , Michael Rack , Ulrich Schöfl , Siegfried Strathmann , Reinhard Stierl , Jan Rether
IPC分类号： C07D333/22 , C07C333/32 , A01N25/00 , C07C335/00 , A01N25/32
CPC分类号： C07D333/38
摘要： The invention relates to novel biphenyl carboxamides of formula (I), wherein A, R, Z, X, Y, m and n have the meanings given in the description, to multiple methods for producing these substances, to their use for combating unwanted micro-organisms and to novel intermediate products and the production thereof.
摘要翻译：本发明涉及式（I）的新型联苯甲酰胺，其中A，R，Z，X，Y，m和n具有与本说明书中给出的含义相同的多种生产这些物质的方法，用于防治不想要的微生物和新颖的中间产品及其生产。

12. 发明授权

US07786043B2 2-(pyridin-2-yl)-pyrimidines and their use for controlling harmful fungi 失效
标题翻译： 2-（吡啶-2-基） - 嘧啶及其用于控制有害真菌的用途
公开(公告)号：US07786043B2
公开(公告)日：2010-08-31
申请号：US11632342
申请日：2005-07-22
申请人： Wassilios Grammenos , Thomas Grote , Carsten Blettner , Markus Gewehr , Udo Hünger , Bernd Müller , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Ulrich Schöfl , Harald Köhle , Siegfried Strathmann , Maria Scherer , Reinhard Stierl , Jan Rether
发明人： Wassilios Grammenos , Thomas Grote , Carsten Blettner , Markus Gewehr , Udo Hünger , Bernd Müller , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Ulrich Schöfl , Harald Köhle , Siegfried Strathmann , Maria Scherer , Reinhard Stierl , Jan Rether
IPC分类号： C07D239/74 , C07D239/70 , C07D401/04 , C07D403/04 , A01N43/54 , C07D213/16 , C07D213/84 , C07D213/53 , C07D213/61 , C07D213/26
CPC分类号： C07D401/04
摘要： The invention relates to 2-(pyridin-2-yl)-pyrimidine compounds of general formula (I) and their use for controlling pathogenic fungi and as plant protection products that, as an active constituent, contain compounds of this type: In general formula (I), k represents 0, 1, 2, 3; m represents 0, 1, 2, 3, 4 or 5; n represents 1, 2, 3, 4 or 5; R1, independent of one another, represents halogen, OH, CN, NO2, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, C2-C4 alkenyl, C2-C4 alkynyl, C3-C8 cycloalkyl, C1-C4 alkoxy-C1-C4 alkyl, amino, phenoxy, which is optionally substituted by halogen or C1-C4 alkyl, NHR, NR2, C(Ra)═N—ORb, S(═O)pA1 or C(═O)A2, or two radicals R1 bound to adjacent carbon atoms can, together, also represent a group —O-Alk-O—, wherein Alk represents a linear or branched C1-C4 alkylene, and 1, 2, 3 or 4 hydrogen atoms can also be replaced by halogen; R2 represents C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, hydroxy, halogen, CN or NO2; whereby R2 can also represent hydrogen or C1-C4 alkyl when at least one of the three following conditions is fulfilled: n represents 3, 4 or 5; k represents 1, 2 or 3; if m is not equal to 0, at least one of the radicals R1 represents a radical that differs from halogen, C1-C4 alkyl, C1-C4 alkoxy and C1-C4 alkyl halide, and; R3 represents C1-C4 alkyl.
摘要翻译：本发明涉及通式（I）的2-（吡啶-2-基） - 嘧啶化合物及其用于控制致病真菌的用途，作为作为活性成分的植物保护产品含有这种化合物：通式（I）中，k表示0,1,2,3; m表示0,1,2,3,4或5; n表示1,2,3,4或5; R 1彼此独立地表示卤素，OH，CN，NO 2，C 1 -C 4烷基，C 1 -C 4烷基卤，C 1 -C 4烷氧基，C 1 -C 4烷氧基卤化物，C 2 -C 4烯基，C 2 -C 4炔基， C8环烷基，C1-C4烷氧基-C1-C4烷基，氨基，苯氧基，其任选被卤素或C 1 -C 4烷基取代，NHR，NR 2，C（R a）= N-OR b，S（= O）p A1或C （ΟO）A2或与相邻碳原子结合的两个基团R1一起也可以代表基团-O-Alk-O-，其中Alk表示直链或支链C 1 -C 4亚烷基，和1,2,3或 4个氢原子也可以被卤素取代; R2代表C1-C4烷基卤，C1-C4烷氧基，C1-C4烷氧基卤化物，羟基，卤素，CN或NO2; 其中当满足以下三个条件中的至少一个时，R2还可以表示氢或C1-C4烷基：n表示3,4或5; k表示1,2或3; 如果m不等于0，则基团R1中的至少一个表示与卤素，C 1 -C 4烷基，C 1 -C 4烷氧基和C 1 -C 4烷基卤化物不同的基团， R3表示C1-C4烷基。

13. 发明授权

US07695728B2 2-substituted pyridines, processes for their preparation and their use for controlling harmful fungi 失效
标题翻译： 2-取代的吡啶，其制备方法及其用于控制有害真菌的用途
公开(公告)号：US07695728B2
公开(公告)日：2010-04-13
申请号：US11630569
申请日：2005-06-18
申请人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwögler , Markus Gewehr , Wassilios Grammenos , Udo Hünger , Bernd Müller , Peter Schäfer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
发明人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwögler , Markus Gewehr , Wassilios Grammenos , Udo Hünger , Bernd Müller , Peter Schäfer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： C07D401/04 , C07D213/61 , C07D417/04 , C07D213/70 , C07D213/86 , C07D213/78 , A01N43/40
CPC分类号： C07D401/04 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/653 , A01N43/78 , C07D213/61 , C07D213/70 , C07D213/74 , C07D213/78 , C07D213/84 , C07D213/86 , C07D417/04
摘要： The invention relates to 2-substituted pyridines of the formula I in which the index n and the substituents R1 to R4 and L are as defined in the description and in each case one of the two ring members X1, X2 is N, the other is C—H or C-halogen; Y is a group —CH—R1—, —N—R1—, —O— or —S— and is five- or six-membered hetaryl comprising 1 to 3 heteroatoms selected from the group consisting of O, N and S or is phenyl, and to processes for their preparation, intermediates for their preparation, pesticidal compositions and methods for controlling harmful fungi and animal pests using the compounds according to the invention.
摘要翻译：本发明涉及式I中的2-取代吡啶，其中指数n和取代基R 1至R 4和L如说明书中所定义，并且在每种情况下，两个环成员X1，X2中的一个为N，另一个为 C-H或C-卤素; Y是基团-CH-R 1，-N-R 1，-O-或-S-，是包含1至3个选自O，N和S的杂原子的五元或六元杂芳基，或者是苯基，及其制备方法，其制备中间体，杀虫组合物和使用本发明化合物控制有害真菌和动物害虫的方法。

14. 发明申请

US20100286175A1 2-(Pyridin-2-yl)-pyrimidines and Their Use for Controlling Harmful Fungi 审中-公开
标题翻译： 2-（吡啶-2-基） - 嘧啶及其用于控制有害真菌的用途
公开(公告)号：US20100286175A1
公开(公告)日：2010-11-11
申请号：US12840392
申请日：2010-07-21
申请人： Wassilios Grammenos , Thomas Grote , Carsten Blettner , Markus Gewehr , Udo Hünger , Bernd Müller , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Ulrich Schöfl , Harald Köhle , Siegfried Strathmann , Maria Scherer , Reinhard Stierl , Jan Rether
发明人： Wassilios Grammenos , Thomas Grote , Carsten Blettner , Markus Gewehr , Udo Hünger , Bernd Müller , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Ulrich Schöfl , Harald Köhle , Siegfried Strathmann , Maria Scherer , Reinhard Stierl , Jan Rether
IPC分类号： A01N43/54 , C07D401/04 , A01P3/00
CPC分类号： C07D401/04
摘要： The invention relates to 2-(pyridin-2-yl)-pyrimidine compounds of general formula (I) and their use for controlling pathogenic fungi and as plant protection products that, as an active constituent, contain compounds of this type: In general formula (I), k represents 0, 1, 2, 3; m represents 0, 1, 2, 3, 4 or 5; n represents 1, 2, 3, 4 or 5; R1, independent of one another, represents halogen, OH, CN, NO2, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, C2-C4 alkenyl, C2-C4 alkynyl, C3-C8 cycloalkyl, C1-C4 alkoxy-C1-C4 alkyl, amino, phenoxy, which is optionally substituted by halogen or C1-C4 alkyl, NHR, NR2, C(Ra)═N—ORb, S(═O)pA1 or C(═O)A2, or two radicals R1 bound to adjacent carbon atoms can, together, also represent a group —O-Alk-O—, wherein Alk represents a linear or branched C1-C4 alkylene, and 1, 2, 3 or 4 hydrogen atoms can also be replaced by halogen; R2 represents C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, hydroxy, halogen, CN or NO2; whereby R2 can also represent hydrogen or C1-C4 alkyl when at least one of the three following conditions is fulfilled: n represents 3, 4 or 5; k represents 1, 2 or 3; if m is not equal to 0, at least one of the radicals R1 represents a radical that differs from halogen, C1-C4 alkyl, C1-C4 alkoxy and C1-C4 alkyl halide, and; R3 represents C1-C4 alkyl.
摘要翻译：本发明涉及通式（I）的2-（吡啶-2-基） - 嘧啶化合物及其用于控制致病真菌的用途，作为作为活性成分的植物保护产品含有这种化合物：通式（I）中，k表示0,1,2,3; m表示0,1,2,3,4或5; n表示1,2,3,4或5; R 1彼此独立地表示卤素，OH，CN，NO 2，C 1 -C 4烷基，C 1 -C 4烷基卤，C 1 -C 4烷氧基，C 1 -C 4烷氧基卤化物，C 2 -C 4烯基，C 2 -C 4炔基， C8环烷基，C1-C4烷氧基-C1-C4烷基，氨基，苯氧基，其任选被卤素或C 1 -C 4烷基取代，NHR，NR 2，C（R a）= N-OR b，S（= O）p A1或C （ΟO）A2或与相邻碳原子结合的两个基团R1一起也可以代表基团-O-Alk-O-，其中Alk表示直链或支链C 1 -C 4亚烷基，和1,2,3或 4个氢原子也可以被卤素取代; R2代表C1-C4烷基卤，C1-C4烷氧基，C1-C4烷氧基卤化物，羟基，卤素，CN或NO2; 其中当满足以下三个条件中的至少一个时，R2还可以表示氢或C1-C4烷基：n表示3,4或5; k表示1,2或3; 如果m不等于0，则基团R1中的至少一个表示与卤素，C 1 -C 4烷基，C 1 -C 4烷氧基和C 1 -C 4烷基卤化物不同的基团， R3表示C1-C4烷基。

15. 发明申请

US20060211711A1 7-(Alkinylamino)-triazolopyrimidines, methods for the production and use thereof to combat harmful fungi and agents containing said compounds 审中-公开
标题翻译： 7-（烷基氨基） - 三唑并嘧啶，其生产和使用方法，用于对付有害真菌和含有所述化合物的试剂
公开(公告)号：US20060211711A1
公开(公告)日：2006-09-21
申请号：US10550571
申请日：2004-03-30
申请人： Jordi Blasco , Carsten Blettner , Bernd Müller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
发明人： Jordi Blasco , Carsten Blettner , Bernd Müller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： A61K31/519 , C07D487/04 , A01N43/90
CPC分类号： C07D487/04 , A01N43/90
摘要： 7-alkinylamino-triazolopyrimidins of formula (I), wherein the substituents have the following meanings: L=halogen, alkyl, halogenalkyl, alkoxy, amino, NHR, NR2, cyano, S(O)nA1 or C(O)A2; R=alkyl or alkylcarbonyl, A1=hydrogen, hydroxy, alkyl, alkylamino or aialkylamino; n=0, 1 or 2; A2=alkenyl, alkoxy, halogenalkoxy or one of the groups cited in A1; m=1, 2, 3, 4 or 5, whereby at least one group L is present in an ortho-position to the bond with the triazolopyrimidine skeleton; X=halogen, cyano, alkyl, halogenalkyl or alkoxy; R1=hydrogen or alkyl; R2=alkinyl which can be unsubstituted or substituted according to the description. The invention also relates to methods for the production of said compounds, agents containing said compounds and the use thereof to combat harmful phytopathogenic fungi.
摘要翻译：式（I）的7-烷基氨基 - 三唑并嘧啶类，其中取代基具有以下含义：L =卤素，烷基，卤代烷基，烷氧基，氨基，NHR，NR 2，氰基，S（O）或者C（O）A 2 O 2。 R =烷基或烷基羰基，A 1〜H 2，羟基，烷基，烷基氨基或亚烷基氨基; n = 0,1或2; 链烯基，烷氧基，卤代烷氧基或A 1中引用的基团之一; m = 1,2,3,4或5，其中至少一个基团L存在于与三唑并嘧啶骨架的键的邻位; X =卤素，氰基，烷基，卤代烷基或烷氧基; R 1 =氢或烷基; R 2 =炔基，其可以是未取代的或根据描述取代的。本发明还涉及生产所述化合物的方法，含有所述化合物的试剂及其用于对抗有害植物病原真菌的用途。

16. 发明申请

US20060217400A1 Triazolopyrimidines, methods for the production thereof, use thereof for controlling harmful fungi, and substances containing said triazolopyrimidines 审中-公开
标题翻译：三唑并嘧啶类，其生产方法，用于控制有害真菌的用途以及含有所述三唑并嘧啶的物质
公开(公告)号：US20060217400A1
公开(公告)日：2006-09-28
申请号：US10539559
申请日：2003-12-17
申请人： Bernd Müller , Jordi Blasco , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Eberhard Ammermann , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
发明人： Bernd Müller , Jordi Blasco , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Eberhard Ammermann , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： A01N43/90 , C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： Triazolopyrimidines of the formula I in which the index n and the substituents R1, R2 and R3 are as defined in the description, and processes for preparing these compounds, compositions comprising them and their use for controlling harmful fungi are described.
摘要翻译：其中指数n和取代基R 1，R 2和R 3的式I的三唑并嘧啶如说明书中所定义，以及描述了制备这些化合物的方法，包含它们的组合物及其用于控制有害真菌的用途。

17. 发明申请

US20060293314A1 4- Piridinylmethylsulphonamide derivatives as fungicidal plant protein agents 失效
标题翻译： 4-吡啶基甲基磺酰胺衍生物作为杀真菌植物蛋白剂
公开(公告)号：US20060293314A1
公开(公告)日：2006-12-28
申请号：US10570893
申请日：2004-09-10
申请人： Wassilos Grammenos , Carsten Blettner , Bernd Müller , Marker Gewehr , Jordi Blasco , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwögler , Oliver Wagner , Norbert Gotz , Siegfried Strathmann , Ulrich Schöfl , Maria Scherer , Reinhard Stierl
发明人： Wassilos Grammenos , Carsten Blettner , Bernd Müller , Marker Gewehr , Jordi Blasco , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwögler , Oliver Wagner , Norbert Gotz , Siegfried Strathmann , Ulrich Schöfl , Maria Scherer , Reinhard Stierl
IPC分类号： A61K31/541 , A61K31/5377 , A61K31/496 , A61K31/4439 , A61K31/44 , C07D417/02 , C07D403/02 , C07D413/02
CPC分类号： C04B35/632 , C07D213/42 , C07D215/12 , C07D401/12 , C07D409/12
摘要： Sulfonamides of the formula I where the substituents are as follows: R1 is hydrogen, alkyl, alkoxy, alkenyl or alkynyl; and R2, R3, R4, R5 are hydrogen, halogen, alkyl, alkoxy or halomethyl; R2 and R3 together may also form a phenyl, cyclopentyl or cyclohexyl ring, it being possible for these rings to carry two groups R2, and R3,, R2,, R3, are hydrogen, halogen, alkyl, alkoxy or halomethyl; in case a), if R2, R3, R4 and R5 are hydrogen: X is phenyl substituted by a group —C(R6)═NOR7, where R6 is alkyl and R7 is alkyl, benzyl, alkenyl, haloalkyl, haloalkenyl, alkynyl or haloalkynyl; and in case b), if at least one of the groups R2, R3, R4 and R5 is not hydrogen: X is phenyl, naphthyl or a five- or six-membered saturated, or partially unsaturated or aromatic heterocycle which is attached via a carbon atom and contains one to four heteroatoms from the group consisting of O, N and S, where X may be substituted according to the description; Processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：式I的磺酰胺，其中取代基如下：R 1是氢，烷基，烷氧基，烯基或炔基; R 2，R 3，R 4，R 5是氢，卤素，烷基，烷氧基或卤代甲基 ; R 2和R 3一起也可以形成苯基，环戊基或环己基环，这些环可以携带两个基团R 2， R 3，R 3，R 3，R 3，R 3，R 3和R 3分别为氢，卤素，烷基，烷氧基或卤代甲基; 在a）情况下，如果R 2，R 3，R 4和R 5是氢：X是由基团-C（R 6） - NOR 7取代的苯基，其中R 6为烷基，R 7为H 烷基，苄基，烯基，卤代烷基，卤代烯基，炔基或卤代炔基; 并且在情况b）中，如果R 2，R 3，R 4和R 5中的至少一个， SUP>不是氢：X是苯基，萘基或五或六元饱和或部分不饱和或芳族杂环，其通过碳原子连接并含有一至四个由O，N和S组成的组的杂原子，其中X可以根据描述被替代; 制备这些化合物的方法，包含它们的组合物及其用于控制植物病原性有害真菌的用途。

18. 发明授权

US07601673B2 Fungicidal mixtures 有权
标题翻译：杀菌混合物
公开(公告)号：US07601673B2
公开(公告)日：2009-10-13
申请号：US11579085
申请日：2005-04-23
申请人： Jordi Tormo I Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl , Markus Gewehr , Bernd Müller , Miguel Octavio Suarez-Cervieri , Matthias Niedenbrück
发明人： Jordi Tormo I Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl , Markus Gewehr , Bernd Müller , Miguel Octavio Suarez-Cervieri , Matthias Niedenbrück
IPC分类号： A01N25/00 , A01N59/04
CPC分类号： A01N43/653 , A01N35/04 , A01N37/20 , A01N37/24 , A01N37/34 , A01N37/36 , A01N37/52 , A01N43/16 , A01N43/40 , A01N43/42 , A01N43/54 , A01N43/78 , A01N43/86 , A01N43/90 , A01N47/04 , A01N47/12 , A01N47/18 , A01N47/20 , A01N47/38
摘要： Fungicidal mixtures, comprising, as active components, 1) a sulfamoyl compound of the formula I, in which the substituents are as defined below: R1 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkoxy, alkylthio, alkoxycarbonyl, phenyl, benzyl, formyl or CH═NOA; A is hydrogen, alkyl, alkylcarbonyl; R2 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkoxycarbonyl; R3 is halogen, cyano, nitro, alkyl, haloalkyl, alkoxy, alkylthio, alkoxycarbonyl, formyl or CH═NOA; n is 0, 1, 2, 3 or 4; R4 is hydrogen, halogen, cyano, alkyl or haloalkyl; and 2) at least one active compound selected from the following groups: A) azoles; B) strobilurins; C) acylalanines; D) amine derivatives; E) anilinopyrimidines; F) dicarboximides; G) cinnamides and analogs; H) dithiocarbamates; I) heterocylic compounds; K) sulfur and copper fungicides; L) nitrophenyl derivatives; M) phenylpyrroles; N) sulfenic acid derivatives; O) other fungicides; according to the description; in a synergistically effective amount, methods for controlling harmful fungi using mixtures of a compound I with active compounds of groups A) to O) and the use of the compounds I with active compounds of groups A) to O) for preparing such mixtures, and also compositions comprising these mixtures.
摘要翻译：作为活性组分的杀真菌混合物，1）式I的氨磺酰基化合物，其中取代基如下：R 1是氢，卤素，氰基，烷基，卤代烷基，烷氧基，烷硫基，烷氧基羰基，苯基，苄基，甲酰基或CH-NOA; A是氢，烷基，烷基羰基; R2是氢，卤素，氰基，烷基，卤代烷基，烷氧基羰基; R3是卤素，氰基，硝基，烷基，卤代烷基，烷氧基，烷硫基，烷氧基羰基，甲酰基或CH-NOA; n为0,1,2,3或4; R4是氢，卤素，氰基，烷基或卤代烷基; 和2）至少一种选自以下组的活性化合物：A）唑类; B）嗜球果伞素 C）酰基丙氨酸; D）胺衍生物; E）苯胺嘧啶嘧啶; F）二羧酰亚胺; G）肉桂酸酯类似物; H）二硫代氨基甲酸盐; I）杂环化合物; K）硫和铜杀菌剂; L）硝基苯基衍生物; M）苯基吡咯; N）亚磺酸衍生物; O）其他杀菌剂; 根据说明; 协同有效量的方法，使用化合物I与基团A）至O）的活性化合物的混合物控制有害真菌的方法，以及将化合物I与基团A）至O）的活性化合物用于制备此类混合物的用途，以及也包含这些混合物的组合物

19. 发明申请

US20110136665A1 Ternary Fungicidal Mixtures 审中-公开
标题翻译：三元杀真菌混合物
公开(公告)号：US20110136665A1
公开(公告)日：2011-06-09
申请号：US10591290
申请日：2005-03-26
申请人： Jordi Tormo i Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl
发明人： Jordi Tormo i Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl
IPC分类号： A01N43/90 , A01N55/10 , A01P3/00 , A01N25/26
CPC分类号： A01N43/90 , A01N37/50 , A01N47/24 , A01N47/38 , A01N43/40 , A01N43/653 , A01N2300/00
摘要： Ternary fungicidal mixtures comprising, as active components, 1) the triazolopyrimidine derivative of the formula I, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine and 2) a strobilurin derivative II, selected from among the compounds pyraclostrobin and orysastrobin and 3) a fungicidally active compound III selected from the group consisting of acylalanines, amine derivatives, anilinopyrimidines, antibiotics, azoles, dicarboximides, dithiocarbamates, copper fungicides, nitrophenyl derivatives, phenylpyrroles, sulfenic acid derivatives, cinnamides and analogs and anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, famoxadone, fenamidone, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, picobenzamid, probenazole, proquinazid, pyrifenox, pyroquilon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate-methyl, tiadinil, tricyclazole, triforine, sulfur, acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, cymoxanil, dazomet, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid, fosetyl, fosetyl-aluminum, iprovalicarb, hexachlorobenzene, metrafenon, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene and zoxamide; in a synergistically effective amount, methods for controlling phytopathogenic harmful fungi using mixtures of the compounds I and II and III with a fungicidally active compound III and the use of the compounds I and II with III for preparing such mixtures, and also compositions comprising these mixtures.
摘要翻译：作为活性组分的三元杀真菌混合物，1）式I的三唑并嘧啶衍生物，5-氯-7-（4-甲基哌啶-1-基）-6-（2,4,6-三氟苯基） - [ 2,4]三唑并[1,5-a]嘧啶和2）嗜球果伞素衍生物II，选自化合物吡咯菌酯和奥沙曲坦，以及3）杀真菌活性化合物III，其选自酰基丙氨酸，胺衍生物，苯胺基嘧啶，苯并吡喃，苯菌灵，多菌灵，多菌灵，羧苯甲酸，氧car box，，，amid amid，，，，，，on on on，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，，氟虫胺，呋虫胺，异丙硫醇，甲丙酮，阿拉伯胶，吡啶甲酰胺，丙烯三唑，喹喔啉，吡哆醛，焦宁碱，喹诺酮，硫唑啶，噻菌灵，噻吗啉，甲基托布津，噻替尼，三环唑，，苯偶氮-S-甲基，benthiavalicarb，carpropamid，百菌清，cyflufenamid，cymoxanil，dazomet，diclomezin，diclocymet，diethofencarb，edifenphos，ethaboxam，fenhexamid，芬太芬醋酸盐，芬诺昔尼，ferimzone，氟啶胺，亚磷酸，fosetyl，fosetyl铝，六氯苯，metrafenon，pcurcuron，propamocarb，phthalide，toloclofos-methyl，quintozene和zoxamide; 协同有效量的方法，使用化合物I和II和III与杀真菌活性化合物III的混合物来控制植物病原性有害真菌，以及使用化合物I和II与III制备这种混合物，以及包含这些混合物的组合物。

20. 发明授权

US07282503B2 Fungicidal mixtures based on imidazole derivatives 失效
标题翻译：基于咪唑衍生物的杀真菌剂
公开(公告)号：US07282503B2
公开(公告)日：2007-10-16
申请号：US10532769
申请日：2003-11-14
申请人： Jordi Tormo i Blasco , Thomas Grote , Eberhard Ammermann , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl
发明人： Jordi Tormo i Blasco , Thomas Grote , Eberhard Ammermann , Reinhard Stierl , Siegfried Strathmann , Ulrich Schöfl
IPC分类号： A01N43/50 , A01N43/76 , A01N43/80 , A01N43/90
CPC分类号： A01N43/90 , A01N2300/00
摘要： Disclosed are fungicidal mixtures containing a synergistically effective amount of A) a triazolopyrimidine of formula I, and B) imidazole derivatives of formula II, wherein X1 and X2 represent halogen and phenyl which can be substituted by halogen or alkyl, or X1 and X2 form a difluoromethylendioxyphenyl group along with the bridging C═C double bond, X3 represents cyano or halogen, and X4 represents dialkylamino or isoxazol-4yl that can carry two alkyl radicals. The invention also relates to methods for controlling destructive fungi by means of mixtures of compounds I and II, agents containing said mixtures, and the use of compounds I and II for producing such mixtures.
摘要翻译：公开了含有协同有效量的A）式I的三唑并嘧啶和B）式II的咪唑衍生物的杀真菌混合物，其中X 1和X 2代表卤素和可被卤素或烷基取代的苯基或X 1和X 2 2与桥连CC双键一起形成二氟甲基内酰氧基苯基，X 3 O >表示氰基或卤素，X 4表示可带有两个烷基的二烷基氨基或异恶唑-4-基。本发明还涉及通过化合物I和II的混合物控制破坏性真菌的方法，含有所述混合物的试剂以及化合物I和II用于制备这种混合物的方法。

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