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1. 发明授权

US08679514B2 Fungicidal mixtures based on azolopyrimidinylamines 有权
标题翻译：基于偶氮嘧啶胺的杀真菌混合物
公开(公告)号：US08679514B2
公开(公告)日：2014-03-25
申请号：US11996608
申请日：2006-07-20
申请人： Christine Beck , Matthias Niedenbrück , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Udo Hünger
发明人： Christine Beck , Matthias Niedenbrück , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Udo Hünger
IPC分类号： A01N43/90 , A01P3/00 , A01N59/20 , A01N47/24 , A01N47/14 , A01N47/12 , A01N47/04 , A01N43/88 , A01N43/76 , A01N43/653 , A01N43/54 , A01N43/50 , A01N43/40 , A01N37/50 , A01N37/46
CPC分类号： A01N43/90 , A01N2300/00
摘要： Fungicidal mixtures comprising, as active components, 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined in the description and 2) at least one active compound II selected from the following groups: azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines, antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; in a synergistically effective amount. Methods for controlling harmful fungi using mixtures of the compound I with active compounds II and the use of the compound I with active compounds II 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包括：1）式I的唑并嘧啶基胺，其中取代基如说明书中所定义，以及2）至少一种选自以下基团的活性化合物II：唑类，嗜球半胱氨酸，甲酰胺，杂环化合物，氨基甲酸酯和其它选自胍基，抗生素，含硫杂环基化合物，有机磷化合物，有机氯化合物，无机活性化合物，生长阻滞剂和环氟酰胺胺，胞嘧菌胺，二甲苯咪唑，乙苯咪唑，呋拉西林，甲泼尼龙和螺螺胺的活性化合物; 协同有效量。使用化合物I与活性化合物II的混合物和使用化合物I与活性化合物II制备这种混合物的方法来控制有害真菌的方法，以及包含这些混合物的组合物。

2. 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。

3. 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。

4. 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。

5. 发明授权

US07820647B2 2-substituted pyrimidines and their use as pesticides 失效
标题翻译： 2-取代嘧啶及其作为农药的用途
公开(公告)号：US07820647B2
公开(公告)日：2010-10-26
申请号：US11596891
申请日：2005-05-17
申请人： Anja Schwögler , Frank Schieweck , Joachim Rheinheimer , Markus Gewehr , Bernd Müller , Thomas Grote , Wassilios Grammenos , Udo Hünger , Carsten Blettner , Peter Schäfer , Oliver Wagner , Reinhard Stierl , Ulrich Schöfl , Siegfried Strathmann , Maria Scherer
发明人： Anja Schwögler , Frank Schieweck , Joachim Rheinheimer , Markus Gewehr , Bernd Müller , Thomas Grote , Wassilios Grammenos , Udo Hünger , Carsten Blettner , Peter Schäfer , Oliver Wagner , Reinhard Stierl , Ulrich Schöfl , Siegfried Strathmann , Maria Scherer
IPC分类号： C07D239/48 , C07D403/04 , A01N43/54 , A01N43/58 , A01N43/34 , A01P3/00
CPC分类号： C07D401/04 , C07D403/04
摘要： The invention relates to 2-substituted pyrimidines of the formula I in which the index n and the substituents L and R1 to R3 are as defined in the description and X is a group —CH—Ra, —N—Rb—, —O— or —S—; Ra may be hydrogen, halogen, C1-C6-alkyl, C1-C6-alkoxy, cyano or C1-C6-alkoxycarbonyl; Rb is hydrogen, C1-C6-alkyl or C3-C6-cycloalkyl; T is a group —CH—Ra—; p is an integer from 1 to 4; Y is a group —CH—Ra— or —N—Rb—, o is 0 or 1; Z is O, S or a group N(Rc) Rc is hydrogen, C1-C6-alkyl or C1-C6-alkoxy, and to processes for their preparation, to pesticidal compositions comprising them and to their use as pesticides.
摘要翻译：本发明涉及式I的2-取代嘧啶，其中指数n和取代基L和R1至R3如说明书中所定义，X为基团-CH-Ra，-N-Rb-，-O- 或-S-; R a可以是氢，卤素，C 1 -C 6 - 烷基，C 1 -C 6 - 烷氧基，氰基或C 1 -C 6 - 烷氧基羰基; R b是氢，C 1 -C 6 - 烷基或C 3 -C 6 - 环烷基; T是基团-CH-R a; p是1至4的整数; Y是基团-CH-R a或-N-R b - ，o是0或1; Z是O，S或基团N（R c）R c是氢，C 1 -C 6烷基或C 1 -C 6 - 烷氧基，并且其制备方法，包含它们的杀虫组合物和它们作为农药的用途。

6. 发明授权

US09487519B2 5,6-Dialkyl-7-aminotriazolopyrimidines, their preparation and their use for controlling harmful fungi, and compositions comprising these compounds 有权
标题翻译： 5,6-二烷基-7-氨基三唑并嘧啶，它们的制备及其用于控制有害真菌的用途，以及包含这些化合物的组合物
公开(公告)号：US09487519B2
公开(公告)日：2016-11-08
申请号：US10589953
申请日：2005-03-08
申请人： Jordi Tormo i Blasco , Carsten Blettner , Bernd Müller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Oliver Wagner , Matthias Niedenbrück , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
发明人： Jordi Tormo i Blasco , Carsten Blettner , Bernd Müller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schäfer , Frank Schieweck , Anja Schwögler , Oliver Wagner , Matthias Niedenbrück , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： C07D487/04
CPC分类号： C07D487/04
摘要： 5,6-Dialkyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl or alkoxyalkyl, where the aliphatic groups may be substituted as defined in the description; R2 is CHR3CH3, cyclopropyl, CH═CH2 or CH2CH═CH2; R3 is hydrogen, CH3 or CH2CH3; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

7. 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

8. 发明申请

US20080200334A1 Method For Enhancing The Effectiveness Of Ethaboxam 审中-公开
标题翻译：提高乙异唑的有效性的方法
公开(公告)号：US20080200334A1
公开(公告)日：2008-08-21
申请号：US11791191
申请日：2005-11-23
申请人： Jordi Tormo I Blasco , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Matthias Niedenbruck , Horst Dieter Brix , Markus Gewehr , Christine Beck
发明人： Jordi Tormo I Blasco , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Matthias Niedenbruck , Horst Dieter Brix , Markus Gewehr , Christine Beck
IPC分类号： A01N25/26 , A01N43/78 , A01N43/84 , A01N43/32 , A01N43/56 , A01P3/00
CPC分类号： A01N43/78 , A01N47/04 , A01N2300/00
摘要： Method for enhancing the fungicidal effectiveness of a) ethaboxam of the formula I, which comprises applying the active compound I simultaneously, that is separately or together, with at least one active compound II from the group consisting of: b) dithiocarbamates, such as maneb, mancozeb, metam or metiram, sulfenic acid derivatives, such as captan or folpet, strobilurin derivatives, such as kresoxim-methyl or pyraclostrobin, cinnamides and analogs, such as dimethomorph or flumorph, or dithianon, famoxadone, cymoxanil, fluazinam, zoxamide, mefenoxam or chlorothalonil, N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-ethanesulfonylamino-3-methylbutyramide or 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine in synergistically effective amounts, by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants, no polyoxyalkylene alkyl ether being used as adjuvants, novel synergistic mixtures of ethaboxam and also compositions comprising these mixtures, and the use of ethaboxam for preparing such mixtures.
摘要翻译：提高a）式I的ethaboxam的方法，其包括将活性化合物I同时与另一种或一起与至少一种活性化合物II一起施用，所述活性化合物II来自以下组中的至少一种活性化合物II：b）二硫代氨基甲酸盐，例如maneb ，代森锰锌，metam或metiram，磺酸衍生物，例如克虏伯或派生物，嗜球果伞形毒素衍生物，例如甲氧基甲基或嘧菌酯，肉桂酸酯和类似物，例如烯酰吗啉或氟吗啉，或二噻尼龙，恶唑酮，胞嘧啶，氟啶胺，唑酰胺，或百菌清，N-（2- {4- [3-（4-氯苯基）丙-2-炔基氧基] -3-甲氧基苯基}乙基）-2-甲磺酰基氨基-3-甲基丁酰胺，N-（2- {4- [ 3-（4-氯苯基）丙-2-炔基氧基] -3-甲氧基苯基}乙基）-2-乙磺酰基氨基-3-甲基丁酰胺或5-氯-7-（4-甲基哌啶-1-基）-6-（2， 4,6-三氟苯基） - [1,2,4]三唑并[1,5-a]嘧啶，具有协同有效的量，通过在或之前喷洒或除尘种子，植物或土壤 r播种植物或在植物出现之前或之后，不使用聚氧亚烷基烷基醚作为佐剂，含有这些混合物的组合物的ethaboxam的新型协同混合物，以及使用ethaboxam制备这些混合物。

9. 发明申请

US20080234295A1 Fungicidal Mixtures Based on Azolopyrimidinylamines 有权
标题翻译：基于偶氮嘧啶胺的杀真菌剂
公开(公告)号：US20080234295A1
公开(公告)日：2008-09-25
申请号：US11996608
申请日：2006-07-20
申请人： Christine Beck , Matthias Niedenbruck , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Udo Hunger
发明人： Christine Beck , Matthias Niedenbruck , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Udo Hunger
IPC分类号： A01N43/90 , A01N25/34 , A01P3/00
CPC分类号： A01N43/90 , A01N2300/00
摘要： Fungicidal mixtures comprising, as active components,1) azolopyrimidinylamines of the formula I, in which the substituents are as defined in the description and 2) at least one active compound II selected from the following groups: azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines, antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; in a synergistically effective amount. Methods for controlling harmful fungi using mixtures of the compound I with active compounds II and the use of the compound I with active compounds II 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包括：1）式I的唑并嘧啶基胺，其中取代基如说明书中所定义，以及2）至少一种选自以下基团的活性化合物II：唑类，嗜球半胱氨酸，甲酰胺，杂环化合物，氨基甲酸酯和其它选自胍基，抗生素，含硫杂环基化合物，有机磷化合物，有机氯化合物，无机活性化合物，生长阻滞剂和环氟酰胺胺，胞嘧菌胺，二甲苯咪唑，乙苯咪唑，呋拉西林，甲泼尼龙和螺螺胺的活性化合物; 协同有效量。使用化合物I与活性化合物II的混合物和使用化合物I与活性化合物II制备这种混合物的方法来控制有害真菌的方法，以及包含这些混合物的组合物。

10. 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。

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