HEXAHYDROPYRANO[3,4-d][1,3]THIAZIN-2-AMINE COMPOUNDS
    31.
    发明申请
    HEXAHYDROPYRANO[3,4-d][1,3]THIAZIN-2-AMINE COMPOUNDS 有权
    四氢呋喃并[3,4-d] [1,3]噻嗪-2-胺化合物

    公开(公告)号:US20140163015A1

    公开(公告)日:2014-06-12

    申请号:US14101462

    申请日:2013-12-10

    Applicant: Pfizer Inc.

    CPC classification number: A61K31/542 C07D513/04

    Abstract: The present invention provides compounds of Formula I, and the tautomers thereof, and the pharmaceutically acceptable salts of the compounds and tautomers, wherein the compounds have the structure wherein the variables R1, R2, R3, R4 and x are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    Abstract translation: 本发明提供式I化合物及其互变异构体,以及化合物和互变异构体的药学上可接受的盐,其中化合物具有其中变量R1,R2,R3,R4和x如说明书中所定义的结构。 还公开了相应的药物组合物,治疗方法,合成方法和中间体。

    Alkyl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
    37.
    发明授权
    Alkyl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds 有权
    烷基取代的六氢吡喃并[3,4-d] [1,3]噻嗪-2-胺化合物

    公开(公告)号:US09260455B2

    公开(公告)日:2016-02-16

    申请号:US14429215

    申请日:2013-09-09

    Applicant: Pfizer Inc.

    CPC classification number: C07D513/04

    Abstract: Compounds, tautomers and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I, wherein the variables R1 and R2 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    Abstract translation: 公开了化合物的化合物,互变异构体和药学上可接受的盐,其中化合物具有式I的结构,其中变量R1和R2如说明书中所定义。 还公开了相应的药物组合物,治疗方法,合成方法和中间体。

    Hexahydropyrano[3,4-d][1,3]Thiazin-2-Amine Compounds
    38.
    发明申请
    Hexahydropyrano[3,4-d][1,3]Thiazin-2-Amine Compounds 审中-公开
    六氢吡喃并[3,4-d] [1,3]噻嗪-2-胺化合物

    公开(公告)号:US20150231144A1

    公开(公告)日:2015-08-20

    申请号:US14695920

    申请日:2015-04-24

    Applicant: Pfizer Inc.

    CPC classification number: A61K31/542 C07D513/04

    Abstract: The present invention provides compounds of Formula I, and the tautomers thereof, and the pharmaceutically acceptable salts of the compounds and tautomers, wherein the compounds have the structure wherein the variables R1, R2, R3, R4 and x are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    Abstract translation: 本发明提供式I化合物及其互变异构体,以及化合物和互变异构体的药学上可接受的盐,其中化合物具有其中变量R1,R2,R3,R4和x如说明书中所定义的结构。 还公开了相应的药物组合物,治疗方法,合成方法和中间体。

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