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    • 1. 发明申请
    • Pyrazole derivatives and process for the production thereof
    • 吡唑衍生物及其制备方法
    • US20050215797A1
    • 2005-09-29
    • US10521593
    • 2003-07-31
    • Masao NakataniMinoru ItoMasahiro Miyazaki
    • Masao NakataniMinoru ItoMasahiro Miyazaki
    • C07D231/20C07D231/22A61K31/4152C07D231/18
    • C07D231/20C07D231/22
    • The present invention provides pyrazole derivatives useful as production intermediates for isoxazoline derivatives having an excellent herbicidal effect and selectivity between crops and weeds as well as processes for producing the same. The pyrazole derivatives or pharmaceutically acceptable salts thereof which are inventive compounds are represented by the general formula [I] or a salt thereof: wherein R1 represents a C1 to C6 alkyl group, R2 represents a C1 to C3 haloalkyl group, R3 represents a hydrogen atom, a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α, or a formyl group, R4 represents a hydrogen atom or a C1 to C3 haloalkyl group, provided that R4 represents a C1 to C3 haloalkyl group in the case that R3 is a hydrogen or a formyl group, and R4 is a hydrogen group or a C1 to C3 haloalkyl group in the case that R3 is a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α.
    • 本发明提供了可用作具有优异的除草效果和作物和杂草之间的选择性的异恶唑啉衍生物的生产中间体的吡唑衍生物及其制备方法。 作为本发明化合物的吡唑衍生物或其药学上可接受的盐由通式[I]或其盐表示:其中R 1表示C 1至C 6烷基,R 2, / SUP>表示C1至C3卤代烷基,R 3表示氢原子,可被一个或多个选自以下取代基组α的取代基取代的C1至C3烷基,或 甲酰基,R 4表示氢原子或C 1至C 3卤代烷基,条件是R 4表示C 1至C 3卤代烷基, 3是氢或甲酰基,R 4是氢或C1至C3卤代烷基,在R 3是C1的情况下 可以被一个或多个选自以下取代基组α的取代基取代的C 3烷基。
    • 2. 发明授权
    • Pyrazole derivatives and process for the production thereof
    • 吡唑衍生物及其制备方法
    • US07256298B2
    • 2007-08-14
    • US10521593
    • 2003-07-31
    • Masao NakataniMinoru ItoMasahiro Miyazaki
    • Masao NakataniMinoru ItoMasahiro Miyazaki
    • C07D231/18
    • C07D231/20C07D231/22
    • The present invention provides pyrazole derivatives useful as production intermediates for isoxazoline derivatives having an excellent herbicidal effect and selectivity between crops and weeds as well as processes for producing the same.The pyrazole derivatives or pharmaceutically acceptable salts thereof which are inventive compounds are represented by the general formula [I] or a salt thereof: wherein R1 represents a C1 to C6 alkyl group, R2 represents a C1 to C3 haloalkyl group, R3 represents a hydrogen atom, a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α, or a formyl group, R4 represents a hydrogen atom or a C1 to C3 haloalkyl group, provided that R4 represents a C1 to C3 haloalkyl group in the case that R3 is a hydrogen or a formyl group, and R4 is a hydrogen group or a C1 to C3 haloalkyl group in the case that R3 is a C1 to C3 alkyl group which may be substituted with one or more substituents selected from the following substituent group α.
    • 本发明提供了可用作具有优异的除草效果和作物和杂草之间的选择性的异恶唑啉衍生物的生产中间体的吡唑衍生物及其制备方法。 作为本发明化合物的吡唑衍生物或其药学上可接受的盐由通式[I]或其盐表示:其中R 1表示C 1至C 6烷基,R 2, / SUP>表示C1至C3卤代烷基,R 3表示氢原子,可被一个或多个选自以下取代基组α的取代基取代的C1至C3烷基,或 甲酰基,R 4表示氢原子或C 1至C 3卤代烷基,条件是R 4表示C 1至C 3卤代烷基, 3是氢或甲酰基,R 4是氢或C1至C3卤代烷基,在R 3是C1的情况下 可以被一个或多个选自以下取代基组α的取代基取代的C 3烷基。