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1. 发明申请

US20080032889A1 6-(2-Fluorophenyl)-Triazolopyrimidines, Method For The Production Thereof, Use Thereof For Controlling Harmful Fungi, And Agents Containing The Same 审中-公开
标题翻译： 6-（2-氟苯基） - 三唑并嘧啶，其生产方法，用于控制有害真菌及其含有药剂
公开(公告)号：US20080032889A1
公开(公告)日：2008-02-07
申请号：US11630558
申请日：2005-06-14
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/90 , A01C1/06 , C07D487/04
CPC分类号： A01N43/90 , C07D487/04
摘要： Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl, halocycloalkyl, alkenyl, cycloalkyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen, alkyl or one of the groups mentioned under R1; R1 and/or R2 may carry one to four identical or different groups Ra: Ra is chlorine, bromine, iodine, cyano, nitro, hydroxyl, alkyl, alkylcarbonyl, cycloalkyl, alkoxy, haloalkoxy, alkoxycarbonyl, alkylthio, alkylamino, dialkyl-amino, alkenyl, cycloalkenyl, alkenyloxy, haloalkenyloxy, alkynyl, halo-alkynyl, alkynyloxy, haloalkynyloxy, cycloalkoxy, cycloalkenyloxy, oxyalkylenoxy, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, where these aliphatic, alicyclic or aromatic groups for their part may be substituted according to the description; and X is halogen; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：取代基如下定义的式I的取代三唑并嘧啶：R 1是烷基，卤代环烷基，烯基，环烷基，环烯基，卤代环烯基，炔基，卤代炔基或萘基，或五或六元环，包含一至四个由O，N和S组成的组的杂原子的2-元饱和的，部分不饱和的或芳族的杂环，R 2是氢，烷基或R 1上提到的基团之一， / SUP>; R 1和/或R 2可以携带一至四个相同或不同的基团R a是：R a是氯，溴，碘，氰基，硝基，羟基，烷基，烷基羰基，环烷基，烷氧基，卤代烷氧基，烷氧基羰基，烷硫基，烷基氨基，二烷基氨基，烯基，环烯基，烯氧基，卤代烯氧基，炔基，卤代炔基，炔氧基，卤代炔氧基，环烷氧基，环烯氧基，氧亚烷基氧基，萘基，五至十元饱和的部分不饱和或芳族杂环，其包含一至四个由O，N和S组成的组的杂原子，其中这些脂族，脂环族或芳族基团可以根据描述进行替代; X为卤素; 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。

2. 发明申请

US20070208038A1 6-(2-Fluorophenyl)-Triazolopyrimidines, Method for Producing Them, Their use for Controlling Parasitic Fungi and Agents Containing the Same 审中-公开
公开(公告)号：US20070208038A1
公开(公告)日：2007-09-06
申请号：US10594738
申请日：2005-03-26
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Michael Rack , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Michael Rack , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A61K31/519 , C07D487/04 , A01N43/90
CPC分类号： A01N43/90 , C07D487/04
摘要： 6-(2-Fluorophenyl)-triazolopyrimidines of the formula I in which the substituents are as defined below: R1 is C4-C8-alkyl, C4-C8-haloalkyl, substituted C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C5-C8-alkenyl, C2-C8-haloalkenyl, C3-C6-cycloalkenyl, C3-C6-halocycloalkenyl, C2-C8-alkynyl, C2-C8-haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen, C1-C3-alkyl or one of the groups mentioned under R1, R1 and R2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and contain one to three further heteroatoms from the group consisting of O, N and S as ring member, except for piperidin-1-yl optionally substituted by methyl groups; R1 and/or R2 may be substituted according to the description; L1 is chlorine or fluorine; L2 is hydrogen, is, if L1 is fluorine, also fluorine; X is alkyl; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

3. 发明申请

US20070167464A1 Fungicidal mixtures 审中-公开
标题翻译：杀菌混合物
公开(公告)号：US20070167464A1
公开(公告)日：2007-07-19
申请号：US11587130
申请日：2005-04-15
申请人： Jordi Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schofl , Matthias Niedenbruck
发明人： Jordi Blasco , Thomas Grote , Maria Scherer , Reinhard Stierl , Siegfried Strathmann , Ulrich Schofl , Matthias Niedenbruck
IPC分类号： A01N43/90 , A01N43/78 , A01N47/10
CPC分类号： A01N43/90 , A01N47/12 , A01N2300/00
摘要： Fungicidal mixtures comprising, as active components, 1) the triazolopyrimidine derivative of the formula I and 2) at least one valinamide derivative of the formula II in which A is phenyl, naphthyl or benzothiazolyl, these groups being unsubstituted or substituted by methyl or halogen, and R is C1-C4-alkyl, in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with the compound II and the use of the compound I with the compound 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的三唑并嘧啶衍生物和2）至少一种式II的缬氨酰胺衍生物，其中A是苯基，萘基或苯并噻唑基，这些基团是未被取代的或被甲基或卤素取代的，并且R是C 1 -C 4 - C 4 - 烷基，协同有效量，使用化合物I与化合物II的混合物来控制有害真菌的方法以及使用具有用于制备这种混合物的化合物II的化合物I，以及包含这些混合物的组合物。

4. 发明申请

US20070142404A1 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，其制备方法，用于控制致病真菌的用途及含有它们的试剂
公开(公告)号：US20070142404A1
公开(公告)日：2007-06-21
申请号：US10590924
申请日：2005-03-29
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Michael Rack , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Michael Rack , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A61K31/519 , C07D487/04
CPC分类号： A01N43/90 , C07D487/04
摘要： 6-(2,6-Dichlorophenyl)triazolopyrimidines of the formula I in which the substituents are as defined below: R1, R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R1 and R2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain one to three further heteroatoms from the group consisting of O, N and S as ring member and which is substituted according to the description; X is alkyl, cyano, alkoxy, haloalkoxy, alkenyloxy or haloalkenyloxy; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：其中取代基如下定义的式I的6-（2,6-二氯苯基）三唑并嘧啶：R 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，炔基，卤代炔基或苯基，萘基或五元或六元饱和的部分不饱和或芳族杂环，其含有一至四个由O，N和S组成的组的杂原子 R 1和R 2连同它们所连接的氮原子一起也可以形成通过N连接的五元或六元杂环基或杂芳基，并且可以含有一个至三个由O，N和S组成的组的另外的杂原子作为环成员，并且根据描述被取代; X是烷基，氰基，烷氧基，卤代烷氧基，烯氧基或卤代烯氧基; 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。

5. 发明申请

US20080248952A1 Substituted 6-Phenyl-7-Aminotriazolopyrimidines, Method for the Production Thereof, Their Use for Controlling Pathogenic Fungi, and Agents Containing These Compounds 审中-公开
标题翻译：取代的6-苯基-7-氨基三唑并嘧啶，其制备方法，其用于控制致病真菌和含有这些化合物的试剂
公开(公告)号：US20080248952A1
公开(公告)日：2008-10-09
申请号：US11631004
申请日：2005-07-06
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： C07D487/04 , A01N43/90 , A01N25/00
CPC分类号： A01N43/90 , C07D487/04
摘要： Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen or a group R1, R1 and R2 together with the nitrogen atom, to which they are attached, may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and which may comprise one to three further heteroatoms from the groups consisting of O, N and S as ring member and/or may be substituted according to the description; L is fluorine, chlorine or methyl; X is cyano, C1-C4-alkyl, C1-C4-alkoxy or C1-C2-haloalkoxy, where X is not methyl if R1 and R2 together are n-pentylene or 3-methyl-n-pentylene and L is fluorine, or R1 and R2 together are 3-methyl-n-pentylene and L is chlorine; processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：取代基如下定义：式I的取代三唑并嘧啶：R 1是烷基，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，炔基，包含一至四个由O，N和S组成的组的杂原子的五或六元饱和的部分不饱和或芳族杂环，R 2是氢或基团R 1， R 1，R 2和R 2与它们所连接的氮原子一起也可以形成五元或六元杂环基或杂芳基，它们是通过N连接并且其可以包含一个至三个由O，N和S组成的基团的另外的杂原子作为环成员和/或可以根据描述被取代; L是氟，氯或甲基; X是氰基，C 1 -C 4 - 烷基，C 1 -C 4 - 烷氧基或C 1 -C 4 - 如果R 1和R 2一起都是正 - 亚戊基，其中X不是甲基，其中X不是甲基或3-甲基 - 正戊烯，L是氟，R 1和R 2一起是3-甲基 - 正戊烯，L是氯; 制备这些化合物的方法和中间体，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。

6. 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。

7. 发明申请

US20080188530A1 Fungicidal Mixtures 审中-公开
标题翻译：杀菌混合物
公开(公告)号：US20080188530A1
公开(公告)日：2008-08-07
申请号：US11793799
申请日：2005-12-21
申请人： Markus Gewehr , Reinhard Stierl , Matthias Niedenbruck , Udo Hunger
发明人： Markus Gewehr , Reinhard Stierl , Matthias Niedenbruck , Udo Hunger
IPC分类号： A01N43/78 , A01N25/26 , A01P3/00
CPC分类号： A01N37/36 , A01N2300/00
摘要： Fungicidal mixtures, comprising as active components 1) the strobilurin derivative of the formula I, and 2) at least one active compound II selected from the group of the carboxamides in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with active compounds II, the use of the compound I with active compounds II for preparing such mixtures and compositions comprising these mixtures.
摘要翻译：包含作为活性组分的杀真菌混合物1）式I的嗜球果伞苷衍生物和2）以协同有效量选择的至少一种选自羧酰胺的活性化合物II，使用化合物I的混合物控制有害真菌的方法使用活性化合物II，使用化合物I与活性化合物II制备这种混合物和包含这些混合物的组合物。

8. 发明申请

US20070249634A1 Triazolopyrimidine Compounds and Use Thereof for Controlling Harmful Fungi 审中-公开
公开(公告)号：US20070249634A1
公开(公告)日：2007-10-25
申请号：US11597409
申请日：2005-06-08
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bern Muller , Matthias Niedenbruck , Joachim Rheinheimer , Petere Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Liliana Rapado , Michael Rack , Barbara Nave , Maria Schere , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bern Muller , Matthias Niedenbruck , Joachim Rheinheimer , Petere Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Liliana Rapado , Michael Rack , Barbara Nave , Maria Schere , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/90 , A01P3/00
CPC分类号： A01N43/90
摘要： The invention relates to the use of triazolopyrimidines of the formula I In which: R1, R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl, C3-C6-cycloalkynyl, phenyl, naphthyl, or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which contains one, two, three or four heteroatoms from the group consisting of O, N and S, where R1, R2 may be substituted as defined in the description or R1 and R2 together with the nitrogen atom to which they are attached may form five- to eight-membered heterocyclyl or heteroaryl which is attached via nitrogen and may contain one, two or three further heteroatoms from the group consisting of O, N and S as ring members and/or may be substituted as defined in the description; L independently of one another are halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyloxy, cyano, C(═O)A1, S(═O)mA2, NRcRd or NRc—(C═O)—Rd, where A1, A2, Rc, Rd and m are as defined in the description; L1 is halogen, alkyl or haloalkyl; L2 is nitro, a group —C(S)NR3R4, a group —C(═N—OR5)(NR6R7) or a group —C(═N—NR8R9)(NR10OR11); X is halogen, cyano, alkyl, alkoxy, haloalkyl or haloalkoxy; R3, R4, R5, R6, R7, R8, R9, R10 and R11 are independently of one another selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl and alkynyl, where the 4 last-mentioned radicals may be substituted as defined in the description; or R3 and R4, or R6 and R7, or R8 and R9 or R10 and R11 together with the nitrogen atom to which they are attached form a four, five, or six-membered saturated or partially unsaturated ring which may be substituted as defined in the description; n is 0, 1, 2 or 3; and the agriculturally acceptable salts thereof, novel triazolopyrimidines, crop protection compositions comprising at least one compound of the formula I and at least one solid or liquid carrier, and a method for controlling phytopathogenic harmful fungi.

9. 发明授权

US07501383B2 Substituted [1,2,4]triazolo[1,5-a]pyrimidines and their use for controlling harmful fungi 失效
标题翻译：取代的[1,2,4]三唑并[1,5-a]嘧啶及其用于控制有害真菌的用途
公开(公告)号：US07501383B2
公开(公告)日：2009-03-10
申请号：US10590368
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 Niedenbruck , 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 Niedenbruck , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： C07D487/04 , A01N25/02 , A01N25/08 , A01N25/26 , A01N43/90
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: R1 represents alkyl or alkoxyalkyl; R2 represents alkyl, R1 and/or R2 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：本发明涉及式（I）的5,6-二烷基-7-氨基 - 三唑并嘧啶，其中取代基定义如下：R1代表烷基或烷氧基烷基; 根据描述，R 2表示烷基，R 1和/或R 2被取代。本发明还涉及一种生产所述化合物的方法，含有后者的药剂及其用于控制植物致病真菌的用途。

10. 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。

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