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    PYRIDAZINE DERIVATIVES
    4.
    发明申请
    PYRIDAZINE DERIVATIVES 审中-公开
    吡啶衍生物

    公开(公告)号：US20100144674A1

    公开(公告)日：2010-06-10

    申请号：US12447028

    申请日：2007-10-23

    申请人： Stephan Trah ,  Clemens Lamberth ,  Sebastian Wendeborn

    发明人： Stephan Trah ,  Clemens Lamberth ,  Sebastian Wendeborn

    IPC分类号： A01N57/00 ,  C07D237/02 ,  A01N43/58 ,  A01N43/54 ,  A01N43/84 ,  A01P3/00 ,  A01P15/00

    CPC分类号： C07D237/14 ,  A01N43/58 ,  C07D237/08 ,  C07D237/12 ,  C07D307/60 ,  C07D307/79 ,  C07D401/04 ,  C07D401/12 ,  C07D403/04 ,  C07D405/04 ,  C07D405/12 ,  C07D407/04 ,  C07D409/04 ,  C07D409/12 ,  C07D413/04 ,  C07D417/04

    摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R1 is hydrogen, C1-C6alkyl, C1-C8haloalkyl or C3-C6cycloalkyl; R2 is cycloalkyl, cycloalkylalkyl, halocycloalkyl, cycloalkoxy, halocycloalkoxy, cycloalkylalkoxy, halocycloalkylalkoxy, alkoxyalkyl, cycloalkoxyalkoxyalkyl, haloalkoxyalkyl, trialkylsilyl, alkylthioalkyl, haloalkylthioalkyl, cycloalkylthio, halocycloalkylthio, cycloalkylalkylthio, halocycloalkylalkylthio, alkylsulfinylalkyl, alkylsulfonylalkyl, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, C2-C6alkenyl, C2-C6alkynyl, optionally substituted arylsulfonyl, optionally substituted aryloxy, optionally optionally substituted heteroaryloxy, optionally substituted arylthio, optionally substituted heteroarylthio; or R2 together with an adjacent carbon atom forms an optionally substituted fused ring; R3 is an optionally substituted aryl; R4 is hydrogen, halogen, C1-C6alkyl, C1-C6haloalkyl, C1-C8alkoxy, C1-C6haloalkoxy, hydroxy or cyano; and n is a whole number from 1 to 4; or an agrochemically usable salt form thereof.

    摘要翻译： 本发明涉及具有杀微生物活性，特别是杀真菌活性的活性成分的式（I）的新哒嗪衍生物，其中R1是氢，C1-C6烷基，C1-C8卤代烷基或C3-C6环烷基; R 2是环烷基，环烷基烷基，卤代环烷基，环烷氧基，卤代环烷氧基，环烷基烷氧基，卤代环烷基烷氧基，烷氧基烷基，环烷氧基烷氧基烷基，卤代烷氧基烷基，三烷基甲硅烷基，烷硫基烷基，卤代烷硫基烷基，环烷硫基，卤代环烷硫基，环烷基烷硫基，卤代环烷基烷硫基，烷基亚磺酰基烷基，烷基磺酰基烷基，烷基亚磺酰基，卤代烷基亚磺酰基，烷基磺酰基，卤代烷基磺酰基， C 6链烯基，C 2 -C 6炔基，任选取代的芳基磺酰基，任选取代的芳氧基，任选任选取代的杂芳氧基，任选取代的芳硫基，任选取代的杂芳硫基; 或R 2与相邻的碳原子一起形成任选取代的稠环; R3是任选取代的芳基; R4是氢，卤素，C1-C6烷基，C1-C6卤代烷基，C1-C8烷氧基，C1-C6卤代烷氧基，羟基或氰基; n为1〜4的整数; 或其农业化学上可用的盐形式。

    NOVEL PYRIDAZINE DERIVATIVES
    8.
    发明申请
    NOVEL PYRIDAZINE DERIVATIVES 审中-公开
    新的吡咯烷酮衍生物

    公开(公告)号：US20100113457A1

    公开(公告)日：2010-05-06

    申请号：US12447025

    申请日：2007-10-23

    申请人： Stephan Trah ,  Clemens Lamberth ,  Sebastian Wendeborn

    发明人： Stephan Trah ,  Clemens Lamberth ,  Sebastian Wendeborn

    IPC分类号： A01N43/58 ,  C07D237/12 ,  C07D237/14 ,  A01P3/00 ,  A01P1/00

    CPC分类号： C07D237/12 ,  A01N43/58 ,  C07D237/14 ,  C07D237/24

    摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R1 is hydrogen, C1-C6alkyl, C1-C6haloalkyl or C3-C6cycloalkyl; R2 is halogen, nitro, cyano, C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylthio or C1-C4haloalkylthio; R3 is an optionally substituted aryl; R4 is fluoro, cyano, C1-C6haloalkyl, C3-C6cycloalkyl, C1-C6haloalkoxy, C1-C6alkylthio or C1-C6haloalkylthio; and n is a whole number from 1 to 4; or an agrochemically usable salt form thereof.

    摘要翻译： 本发明涉及具有杀微生物活性，特别是杀真菌活性的活性成分的式（I）的新哒嗪衍生物，其中R1是氢，C1-C6烷基，C1-C6卤代烷基或C3-C6环烷基; R 2是卤素，硝基，氰基，C 1 -C 4烷基，C 1 -C 4卤代烷基，C 1 -C 4烷氧基，C 1 -C 4卤代烷氧基，C 1 -C 4烷硫基或C 1 -C 4卤代烷硫基; R3是任选取代的芳基; R 4是氟，氰基，C 1 -C 6卤代烷基，C 3 -C 6环烷基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基或C 1 -C 6卤代烷硫基; n为1〜4的整数; 或其农业化学上可用的盐形式。