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262 条记录 (耗时 0.047 秒)

    Fungicidal N-[2-(Haloalkoxy)Phenyl]Heteroarylcarboxamides
    71.
    发明申请
    Fungicidal N-[2-(Haloalkoxy)Phenyl]Heteroarylcarboxamides 审中-公开
    杀真菌剂N- [2-（卤代烷氧基）苯基]杂芳基甲酰胺

    公开(公告)号：US20100222217A1

    公开(公告)日：2010-09-02

    申请号：US11989973

    申请日：2006-08-02

    申请人： Markus Gewehr ,  Jochen Dietz ,  Thomas Grote ,  Wassilios Grammenos ,  Bernd Müller ,  Jan Klaas Lohmann

    发明人： Markus Gewehr ,  Jochen Dietz ,  Thomas Grote ,  Wassilios Grammenos ,  Bernd Müller ,  Jan Klaas Lohmann

    IPC分类号： A01N25/26 ,  C07D231/40 ,  A01N43/56 ,  C07D277/46 ,  A01N43/78 ,  C07D213/75 ,  A61K31/44 ,  A01P3/00

    CPC分类号： C07D213/02 ,  A01N43/40 ,  A01N43/56 ,  A01N43/78 ,  C07D231/10 ,  C07D277/00 ,  C07D277/02 ,  C07D277/20

    摘要： N-[2-(Haloalkoxy)phenyl]heteroarylcarboxamides of the formula I, where n=0 or 1, Hal=halogen, X=C2-C4-haloalkyl, Het=a pyrazole, thiazole or pyridine radical (a), (b) or (c), where R1=C1-C4-alkyl or C1-C4-haloalkyl, R2=hydrogen or halogen, R3=C1-C4-alkyl or C1-C4-haloalkyl and R5=halogen, C1-C4-alkyl or C1-C4-haloalkyl; except for N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-1,3-dimethylpyrazol-4-yl-carboxamide, N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-3-trifluoromethyl-1-methylpyrazol-4-yl-carboxamide and N-[2-(2,2,2-trifluorethoxy)phenyl]-3-trifluormethyl-1-methylpyrazol-4-yl-carboxamide. A fungicidal composition comprising at least one compound I, the use of the compounds I for preparing a composition suitable for controlling harmful fungi, a method for controlling harmful fungi using the compounds I and also seed comprising at least one compound I.

    摘要翻译： 式I的N- [2-（卤代烷氧基）苯基]杂芳基甲酰胺，其中n = 0或1，Hal =卤素，X = C 2 -C 4 - 卤代烷基，Het =吡唑，噻唑或吡啶基（a），（b ）或（c）中，其中R 1 = C 1 -C 4 - 烷基或C 1 -C 4 - 卤代烷基，R 2 =氢或卤素，R 3 = C 1 -C 4 - 烷基或C 1 -C 4卤代烷基，R 5 =卤素，C 1 -C 4 - 烷基 或C 1 -C 4 - 卤代烷基; 除了N- [2-（1,1,2,2-四氟乙氧基）苯基] -1,3-二甲基吡唑-4-基 - 甲酰胺，N- [2-（1,1,2,2-四氟乙氧基）苯基 ] -3-三氟甲基-1-甲基吡唑-4-基甲酰胺和N- [2-（2,2,2-三氟乙氧基）苯基] -3-三氟甲基-1-甲基吡唑-4-基 - 甲酰胺。 包含至少一种化合物I的杀真菌组合物，使用化合物I制备适于控制有害真菌的组合物，使用化合物I控制有害真菌的方法，还包含至少一种化合物I的种子。

    3-(Pyridin-2-Yl)-[1,2,4]-Triazines as Fungicides
    72.
    发明申请
    3-(Pyridin-2-Yl)-[1,2,4]-Triazines as Fungicides 审中-公开
    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。

    2-(Pyridin-2-Yl)-Pyrimidines for Use as Fungicides
    73.
    发明申请
    2-(Pyridin-2-Yl)-Pyrimidines for Use as Fungicides 审中-公开
    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。