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51. 发明申请

US20080200480A1 Fungicidal 6-Phenyltriazolopyrimidinylamines 审中-公开
标题翻译：杀真菌剂6-苯基三唑并嘧啶胺
公开(公告)号：US20080200480A1
公开(公告)日：2008-08-21
申请号：US11996782
申请日：2006-07-20
申请人： Jochen Dietz , Thomas Grote , Udo Hunger , Jan Klaas Lohmann , Bernd Muller , Jens Renner , Sarah Ulmschneider , Wassilios Grammenos , Joachim Rheinheimer
发明人： Jochen Dietz , Thomas Grote , Udo Hunger , Jan Klaas Lohmann , Bernd Muller , Jens Renner , Sarah Ulmschneider , Wassilios Grammenos , Joachim Rheinheimer
IPC分类号： A01N43/90 , C07D487/04 , A01P3/00
CPC分类号： C07D487/04
摘要： 6-Phenyltriazolopyrimidinylamines of the formula I, in which the substituents are defined 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6-苯基三唑并嘧啶胺，其中取代基根据描述定义，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。

52. 发明申请

US20080188493A1 5,6-Dialkyl-7-Aminoazolopyrimidines, Their Preparation and Their Use For Controlling Harmful Fungi, and Compositions Comprising These Compounds 审中-公开
标题翻译： 5,6-二烷基-7-氨基偶氮嘧啶，它们的制备及其用于控制有害真菌的组合物，以及包含这些化合物的组合物
公开(公告)号：US20080188493A1
公开(公告)日：2008-08-07
申请号：US11885332
申请日：2006-03-01
申请人： Peter Schäfer , Udo Hunger , Maria Scherer , Harald Kohle , Helmut Schiffer , Thomas Grote , Jochen Dietz , Wassilios Grammenos , Jan Klaas Lohmann , Bernd Muller , Joachim Rheinheimer , Frank Schieweck , Anja Schwogler
发明人： Peter Schäfer , Udo Hunger , Maria Scherer , Harald Kohle , Helmut Schiffer , Thomas Grote , Jochen Dietz , Wassilios Grammenos , Jan Klaas Lohmann , Bernd Muller , Joachim Rheinheimer , Frank Schieweck , Anja Schwogler
IPC分类号： A01N43/90 , C07D487/04 , A01N25/26 , A01P3/00
CPC分类号： C07D487/04 , A01N43/90
摘要： 5,6-Dialkyl-7-aminoazolopyrimidines of the formula I in which the substituents are as defined below: R1 is haloalkyl, haloalkoxyalkyl, alkoxyhaloalkyl, alkenyl, haloalkenyl, alkynyl oder haloalkynyl; R2 is alkyl, alkoxyalkyl, alkenyl or alkynyl; where R1 and/or R2 may be substituted according to the description; A is N or CH, and R3 is CH3 and, if A is CH, additionally hydrogen; processes and intermediates 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5,6-二烷基-7-氨基偶氮嘧啶：R 1是卤代烷基，卤代烷氧基烷基，烷氧基卤代烷基，烯基，卤代烯基，炔基，卤代炔基; R 2是烷基，烷氧基烷基，烯基或炔基; 其中R 1和/或R 2可以根据描述被取代; A是N或CH，R 3是CH 3，并且如果A是CH，另外是氢; 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。

53. 发明授权

US08299262B2 Pyridylmethyl-sulfonamide compounds 失效
标题翻译：吡啶基甲基磺酰胺化合物
公开(公告)号：US08299262B2
公开(公告)日：2012-10-30
申请号：US12746086
申请日：2008-11-21
申请人： Wassilios Grammenos , Jan Klaas Lohmann , Thomas Grote , Jochen Dietz , Bernd Mueller , Michael Puhl , Jens Renner , Sarah Ulmschneider , Marianna Vrettou , Joachim Rheinheimer
发明人： Wassilios Grammenos , Jan Klaas Lohmann , Thomas Grote , Jochen Dietz , Bernd Mueller , Michael Puhl , Jens Renner , Sarah Ulmschneider , Marianna Vrettou , Joachim Rheinheimer
IPC分类号： C07D213/62 , A61K31/44
CPC分类号： C07D213/643 , A01N43/40 , A01N43/42 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/78 , A01N43/80 , C07D213/30 , C07D213/69 , C07D213/70 , C07D213/71 , C07D213/74 , C07D213/79 , C07D217/24 , C07D237/14 , C07D237/16 , C07D239/34 , C07D239/54 , C07D239/60 , C07D261/08 , C07D261/12 , C07D277/24 , C07D277/34 , C07D401/12 , C07D413/12 , C07D417/12 , A01N37/34 , A01N43/653 , A01N47/04 , A01N47/24 , A01N2300/00
摘要： The present invention relates to novel pyridylmethyl-sulfonamide compounds of formula (I) where: n is 0 to 4; m is 0 to 4; R1 is halogen, CN, NO2, OH, SH, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, etc.; and/or two radicals R1 together form a fused ring; R2 is H, C1-C4-alkyl, C1-C4-haloalkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C8-cycloalkyl, C1-C4-alkyl-C3-C8-cycloalkyl or benzyl; R3 is halogen, CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; Y is —O—, C1-C4-alkanediyl, —O—CH2—, —CH2—O—, —C(NORn)—, —S—, —S(═O)—, —S(═O)2— or —N(Rn)—; and the N-oxides, and salts thereof and their use for combating phytopathogenic harmful fungi, and also to compositions and seed comprising at least one such compound.
摘要翻译：本发明涉及式（I）的新的吡啶基甲基磺酰胺化合物，其中：n为0至4; m为0〜4; R1是卤素，CN，NO2，OH，SH，C1-C4-烷基，C1-C4卤代烷基，C1-C4-烷氧基，C1-C4-卤代烷氧基等。和/或两个基团R 1一起形成稠环; R2是H，C1-C4-烷基，C1-C4-卤代烷基，C2-C4-烯基，C2-C4-炔基，C3-C8-环烷基，C1-C4烷基-C3-C8-环烷基或苄基; R 3是卤素，CN，NO 2，C 1 -C 4烷基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基或C 1 -C 4卤代烷氧基; Y是-O - ， - C 1 -C 4 - 烷二基，-O-CH 2 - ， - CH 2 -O-，-C（NORn） - ， - S - ， - S（= O） - ， - S（= O）2 - 或-N（Rn） - ; 及其N-氧化物及其盐及其用于防治植物病原性有害真菌的用途，以及包含至少一种此类化合物的组合物和种子。

54. 发明申请

US20110177950A1 Imidazole and Triazole Compounds, Their Use and Agents Containing the Same 审中-公开
标题翻译：咪唑和三唑化合物，它们的用途和含有它们的药剂
公开(公告)号：US20110177950A1
公开(公告)日：2011-07-21
申请号：US13120055
申请日：2009-09-18
申请人： Jochen Dietz , Thomas Grote , Bernd Mueller , Jan Klaas Lohmann , Jens Renner , Sarah Ulmschneider , Alice Glaettli , Marianna Vrettou , Wassilios Grammenos
发明人： Jochen Dietz , Thomas Grote , Bernd Mueller , Jan Klaas Lohmann , Jens Renner , Sarah Ulmschneider , Alice Glaettli , Marianna Vrettou , Wassilios Grammenos
IPC分类号： A01N43/707 , C07D249/08 , A01P13/00 , A01P3/00 , A01P7/04
CPC分类号： C07D249/08 , C07D233/60
摘要： The present invention relates to compounds of the formula I in which the variables have the meanings defined in the claims and in the description.
摘要翻译：本发明涉及式I化合物，其中变量具有权利要求书和说明书中定义的含义。

55. 发明申请

US20090111692A1 3-(Pyridin-2-Yl)-[1,2,4]-Triazines as Fungicides 审中-公开
标题翻译： 3-（吡啶-2-基） - [1,2,4] - 三嗪作为杀真菌剂
公开(公告)号：US20090111692A1
公开(公告)日：2009-04-30
申请号：US12226026
申请日：2007-04-11
申请人： Wassilios Grammenos , Thomas Grote , Jochen Dietz , Jan Klaas Lohmann , Jens Renner , Bernd Muller , Sarah Ulmschneider
发明人： Wassilios Grammenos , Thomas Grote , Jochen Dietz , Jan Klaas Lohmann , Jens Renner , Bernd Muller , Sarah Ulmschneider
IPC分类号： A01N43/707 , C07D401/06 , A01P3/00
CPC分类号： C07D401/04 , A01N43/707 , C07D401/14 , C07D405/14 , C07D409/14
摘要： The invention relates to 3-(pyridin-2-yl)-[1,2,4]-triazines of formula (I) and their use in the control of parasitic fungi and to herbicides that contain said compounds as an effective ingredient thereof. In formula (I), R1, R2 independently represent OH, halogen, NO2, NH2, C1-C8 alkyl, C1-C8 alkoxy, C1-C8 halogenalkyl, C1-C8 halogenalkoxy, C1-C8 alkylamino or di(C1-C8 alkyl)amino, or they form, together with the C atoms to which they are bound, a saturated five-, six- or seven-membered carbocycle or heterocycle, which, in addition to the carbon ring members, has one or two heteroatoms selected from oxygen or sulfur as the ring members, the carbocycle and the heterocycle being unsubstituted or having 1, 2, 3 or 4 C1-C4 alkyl groups as the substituents; R3 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, or halogen; R4 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy or halogen; R5 represents C1-C8 alkyl, C1-C8 halogenalkyl, C1-C8 alkoxy, C1-C8 halogenalkoxy, C3-C8 cycloalkyl, C3-C8 cycloalkyloxy, five- or six-membered heteroaryl, phenyl, phenoxy, benzyl, benzyloxy, five- or six-membered heteroarylmethyl or five- or six-membered heteroaryloxy, said cyclic groups being unsubstituted or having 1, 2, 3, 4 or 5 groups Ra.
摘要翻译：本发明涉及式（I）的3-（吡啶-2-基） - [1,2,4] - 三嗪及其在控制寄生真菌中的用途以及含有所述化合物作为其有效成分的除草剂。在式（I）中，R 1，R 2独立地表示OH，卤素，NO 2，NH 2，C 1 -C 8烷基，C 1 -C 8烷氧基，C 1 -C 8卤代烷基，C 1 -C 8卤代烷氧基，C 1 -C 8烷基氨基或二）氨基，或者它们与它们所键合的C原子一起形成饱和的五元，六元或七元碳环或杂环，其除了碳环成员之外还具有一个或两个选自以下的杂原子：氧或硫作为环成员，碳环和杂环是未取代的或具有1,2,3或4个C 1 -C 4烷基作为取代基; R 3表示氢，C 1 -C 4烷基，C 1 -C 4烷氧基，C 1 -C 4卤代烷基，C 1 -C 4卤代烷氧基，C 3 -C 6环烷基，C 3 -C 6环烷基甲基或卤素; R4表示氢，C1-C4烷基，C1-C4烷氧基，C1-C4卤代烷基，C1-C4卤代烷氧基或卤素; R5表示C1-C8烷基，C1-C8卤代烷基，C1-C8烷氧基，C1-C8卤代烷氧基，C3-C8环烷基，C3-C8环烷氧基，五元或六元杂芳基，苯基，苯氧基，苄基，苄氧基，或六元杂芳基甲基或五元或六元杂芳氧基，所述环状基团是未取代的或具有1,2,3,4或5个基团Ra。

56. 发明申请

US20090105072A1 2-(Pyridin-2-Yl)-Pyrimidines for Use as Fungicides 审中-公开
标题翻译： 2-（吡啶-2-基） - 嘧啶用作杀真菌剂
公开(公告)号：US20090105072A1
公开(公告)日：2009-04-23
申请号：US12225862
申请日：2007-04-11
申请人： Wassilios Grammenos , Thomas Grote , Jochen Dietz , Jan Klaas Lohmann , Jens Renner , Bernd Muller , Sarah Ulmschneider
发明人： Wassilios Grammenos , Thomas Grote , Jochen Dietz , Jan Klaas Lohmann , Jens Renner , Bernd Muller , Sarah Ulmschneider
IPC分类号： A01N43/54 , C07D239/70 , A01P3/00 , C07D491/052
CPC分类号： C07D401/04 , A01N43/54 , A01N43/90 , C07D401/14 , C07D405/14 , C07D409/14 , C07D491/04
摘要： The present invention relates to 2-(pyridin-2-yl)pyrimidines and their use for controlling harmful fungi, and also to crop protection compositions comprising such compounds as effective component. in which: Q is a fused saturated 5-, 6- or 7-membered carbocycle or a 5-, 6- or 7-membered heterocycle which, in addition to the carbon ring members, has one or two heteroatoms selected from the group consisting of oxygen and sulfur as ring members, where the carbocycle and the heterocycle are unsubstituted or have 1, 2, 3 or 4 C1-C4-alkyl groups as substituents; R1 is hydrogen, OH, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy or halogen; R2 is hydrogen, NO2, halogen, C1-C6-alkyl, C3-C6-cycloalkyl, C1-C6-alkoxy, C1-C6-haloalkyl or C1-C6-haloalkoxy; R3 is hydrogen, halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, or C1-C4-haloalkoxy; R4 is phenyl, 5-membered heteroaryl which has 1, 2, 3 or 4 nitrogen atoms or 1 heteroatom selected from the group consisting of oxygen and sulfur and optionally 1, 2 or 3 nitrogen atoms as ring atoms, or 6-membered hetaryl which has 1, 2, 3 or 4 nitrogen atoms as ring members, where phenyl and 5- and 6-membered hetaryl may have 1, 2, 3 or 4 substituents Ra.
摘要翻译：本发明涉及2-（吡啶-2-基）嘧啶及其用于控制有害真菌的用途，还涉及包含有效成分的化合物的作物保护组合物。其中：Q是稠合的饱和的5-，6-或7-元碳环或5-，6-或7-元杂环，其除了碳环成员之外还具有一个或两个选自以下的杂原子：的氧和硫作为环成员，其中碳环和杂环是未取代的或具有1,2,3或4个C 1 -C 4 - 烷基作为取代基; R 1是氢，OH，C 1 -C 4 - 烷基，C 1 -C 4 - 烷氧基，C 1 -C 4卤代烷基，C 1 -C 4卤代烷氧基或卤素; R2是氢，NO2，卤素，C1-C6-烷基，C3-C6-环烷基，C1-C6-烷氧基，C1-C6卤代烷基或C1-C6-卤代烷氧基; R 3是氢，卤素，C 1 -C 4 - 烷基，C 1 -C 4 - 烷氧基，C 1 -C 4卤代烷基或C 1 -C 4卤代烷氧基; R4是苯基，具有1,2,3或4个氮原子的5元杂芳基或选自氧和硫以及任选的1,2或3个氮原子作为环原子的1个杂原子，或6元杂芳基，具有1,2,3或4个氮原子作为环成员，其中苯基和5-和6-元杂芳基可以具有1,2,3或4个取代基R a。

57. 发明申请

US20080221130A1 Fungicidal 5-Methyl-6-Phenylpyrazolopyrimidin-7-Ylamines 审中-公开
标题翻译：杀真菌剂5-甲基-6-苯基吡唑并嘧啶-7-胺
公开(公告)号：US20080221130A1
公开(公告)日：2008-09-11
申请号：US11996783
申请日：2006-07-20
申请人： Jochen Dietz , Wassilios Grammenos , Udo Hunger , Jan Klaas Lohmann , Jens Renner , Joachim Rheinheimer
发明人： Jochen Dietz , Wassilios Grammenos , Udo Hunger , Jan Klaas Lohmann , Jens Renner , Joachim Rheinheimer
IPC分类号： A01N43/90 , C07D487/04 , A01N25/34 , A01P3/00
CPC分类号： C07D487/04
摘要： 5-Methyl-6-phenylpyrazolopyrimidin-7-ylamines of the formula I in which the substituents are defined according to the description, processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：其中取代基根据描述定义的式I的5-甲基-6-苯基吡唑并嘧啶-7-基胺，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。

58. 发明申请

US20080153707A1 Pyrazolecarboxanilides, Process for Their Preparation and Compositions Comprising Them for Controlling Harmful Fungi 有权
标题翻译：吡唑啉酰苯胺，其制备方法和组合物，用于控制有害真菌
公开(公告)号：US20080153707A1
公开(公告)日：2008-06-26
申请号：US11883957
申请日：2006-02-15
申请人： Markus Gewehr , Jochen Dietz , Thomas Grote , Carsten Blettner , Wassilios Grammenos , Udo Hunger , Bernd Muller , Frank Schieweck , Anja Schwogler , Jan Klaas Lohmann , Joachim Rheinheimer , Peter Schafer , Siegfried Strathmann , Reinhard Stierl
发明人： Markus Gewehr , Jochen Dietz , Thomas Grote , Carsten Blettner , Wassilios Grammenos , Udo Hunger , Bernd Muller , Frank Schieweck , Anja Schwogler , Jan Klaas Lohmann , Joachim Rheinheimer , Peter Schafer , Siegfried Strathmann , Reinhard Stierl
IPC分类号： A01N43/56 , C07D231/00 , A01N25/26
CPC分类号： C07D231/14 , A01N43/56
摘要： The present invention relates to pyrazolecarboxanilides I in which the variables are as defined below: n is zero or 2; m is 2 or 3; X1 is fluorine or chlorine; X2 is halogen; Y is CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, methoxy or methylthio; p is zero or 1; R1 is fluorine, chlorine, bromine, C1-C4-alkyl or C1-C4-haloalkyl; R2 is hydrogen or halogen; R3 is hydrogen, methyl or ethyl; W is O or S; with the proviso that, if a) W═O, R1=methyl and R3 is hydrogen, R2 is not fluorine, or b) W═O, n=0, m=2, p=0, R2 and R3 are hydrogen, R1 is not trifluoromethyl or difluoromethyl, to processes for preparing these compounds, to compositions comprising them and to methods for using them for controlling harmful fungi.
摘要翻译：本发明涉及吡唑烷酰苯胺I，其中变量如下：n为0或2; m为2或3; X 1是氟或氯; X 2是卤素; Y是CN，NO 2，C 1 -C 4 - 烷基，C 1 -C 3 - 4 - 卤代烷基，甲氧基或甲硫基; p为零或1; R 1是氟，氯，溴，C 1 -C 4 - C 1-4烷基或C 1 -C 3 - 低级烷基; R 2是氢或卤素; R 3是氢，甲基或乙基; W为O或S; 条件是，如果a）WO，R 1 =甲基和R 3是氢，R 2不是氟，或b） WO，n = 0，m = 2，p = 0，R 2和R 3是氢，R 1不是三氟甲基或二氟甲基，制备这些化合物的方法，包含它们的组合物以及用于控制有害真菌的方法。

59. 发明申请

US20080125445A1 5,6-Dialkyl-7-Amino-Azolopyrimidines, Method For Their Production, Their Use For Controlling Pathogenic Fungi and Agents Containing Said Compounds 审中-公开
标题翻译： 5,6-二烷基-7-氨基 - 偶氮嘧啶，其制备方法，它们用于控制致病真菌和含有所述化合物的试剂
公开(公告)号：US20080125445A1
公开(公告)日：2008-05-29
申请号：US11885359
申请日：2006-03-01
申请人： Peter Schafer , Udo Hunger , Maria Scherer , Harald Kohle , Helmut Schiffer , Thomas Grote , Jochen Dietz , Wassilios Grammenos , Jan Klaas Lohmann , Bernd Muller , Joachim Rheinheimer , Frank Schieweck , Anja Schwogler
发明人： Peter Schafer , Udo Hunger , Maria Scherer , Harald Kohle , Helmut Schiffer , Thomas Grote , Jochen Dietz , Wassilios Grammenos , Jan Klaas Lohmann , Bernd Muller , Joachim Rheinheimer , Frank Schieweck , Anja Schwogler
IPC分类号： A01N43/90 , C07D487/04 , A01P3/00
CPC分类号： C07D487/04
摘要： 5,6-Dialkyl-7-aminoazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl or alkoxyalkyl, R2 is alkyl, where R1 and/or R2 may be substituted according to the description, A is N or CH, and R3 is CH3 and, if A is CH, additionally hydrogen; processes and intermediates 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5,6-二烷基-7-氨基偶氮嘧啶：R 1是烷基或烷氧基烷基，R 2是烷基，其中R 根据描述，可以取代1和/或R 2，A是N或CH，R 3是CH 3 如果A是CH，另外是氢; 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。

60. 发明申请

US20110045974A1 Substituted Triazinylmethyl Sulfonamides 审中-公开
标题翻译：取代的三嗪基甲磺酰胺
公开(公告)号：US20110045974A1
公开(公告)日：2011-02-24
申请号：US12921941
申请日：2009-03-11
申请人： Jochen Dietz , Thomas Grote , Wassilios Grammenos , Bernd Mueller , Jan Klaas Lohmann , Jens Renner , Sarah Ulmschneider , Marianna Vrettou , Alice Glaettli
发明人： Jochen Dietz , Thomas Grote , Wassilios Grammenos , Bernd Mueller , Jan Klaas Lohmann , Jens Renner , Sarah Ulmschneider , Marianna Vrettou , Alice Glaettli
IPC分类号： A01N43/707 , C07D253/065 , C07D253/07 , C07D251/42 , A01N43/66 , A01P3/00
CPC分类号： C07D251/20 , A01N43/68 , A01N43/707 , C07D251/22 , C07D401/12 , C07D401/14 , C07D403/12 , C07D409/12 , C07D409/14 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要： The present invention relates to triazinylmethyl sulfonamides of formula I wherein T, R1, R2, R3, A, Y and D are as defined in the claims and to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to processes and intermediates for preparing these compounds.
摘要翻译：本发明涉及式I的三嗪基甲基磺酰胺，其中T，R 1，R 2，R 3，A，Y和D如权利要求中所定义，和N-氧化物及其盐及其用于对抗有害真菌的用途，以及包含至少一种这样的化合物的组合物和种子。本发明还涉及制备这些化合物的方法和中间体。

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