PROCESSES FOR THE PREPARATION OF 5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID AND ITS DERIVATIVES
    1.
    发明申请
    PROCESSES FOR THE PREPARATION OF 5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID AND ITS DERIVATIVES 有权
    制备5-亚苄基[2.4]庚-6-烯羧酸及其衍生物的方法

    公开(公告)号:US20140187793A1

    公开(公告)日:2014-07-03

    申请号:US14082406

    申请日:2013-11-18

    CPC classification number: C07D209/54

    Abstract: The present invention relates generally to an improved process for the preparation of 5-azaspiro[2.4]heptane-6-carboxylic acid and its derivatives which are useful intermediates in the synthesis of biologically active molecules, especially in the synthesis of hepatits C virus NS5A inhibitors. In particular, the present invention relates to processes and intermediates for the preparation of compounds of formulae (Ia), (Ib) and (Ic):

    Abstract translation: 本发明一般涉及一种制备5-氮杂螺[2.4]庚烷-6-羧酸及其衍生物的改进方法,其在合成生物活性分子中是有用的中间体,特别是在合成肝素C病毒NS5A抑制剂 。 特别地,本发明涉及制备式(Ia),(Ib)和(Ic)化合物的方法和中间体:

    PROCESS FOR PREPARATION OF SULFONYLUREA BILE ACID DERIVATIVES

    公开(公告)号:US20180148469A1

    公开(公告)日:2018-05-31

    申请号:US15826233

    申请日:2017-11-29

    Abstract: The present invention relates to processes for preparing a compound of Formula I: or a pharmaceutically acceptable salt or solvate thereof. These compounds and pharmaceutical compositions are useful as FXR or TGR5 modulators. Specifically, the present invention relates to bile acid derivatives and methods for their preparation and use.The present invention relates to a process for the preparation of a compound (II) and its salts and derivatives which are useful intermediates in the synthesis of biologically active molecules, especially in the synthesis of FXR and TGR5 modulators. The present invention also relates to a process for the preparation of a compound (III) and its diethylamine salt.

    Process for preparation of sulfonylurea bile acid derivatives

    公开(公告)号:US10584145B2

    公开(公告)日:2020-03-10

    申请号:US15826233

    申请日:2017-11-29

    Abstract: The present invention relates to processes for preparing a compound of Formula I: or a pharmaceutically acceptable salt or solvate thereof. These compounds and pharmaceutical compositions are useful as FXR or TGR5 modulators. Specifically, the present invention relates to bile acid derivatives and methods for their preparation and use. The present invention relates to a process for the preparation of a compound (II) and its salts and derivatives which are useful intermediates in the synthesis of biologically active molecules, especially in the synthesis of FXR and TGR5 modulators. The present invention also relates to a process for the preparation of a compound (III) and its diethylamine salt.

    Processes for the preparation of 5-azaspiro[2.4]heptane-6-carboxylic acid and its derivatives
    5.
    发明授权
    Processes for the preparation of 5-azaspiro[2.4]heptane-6-carboxylic acid and its derivatives 有权
    制备5-氮杂螺[2.4]庚烷-6-羧酸及其衍生物的方法

    公开(公告)号:US08927739B2

    公开(公告)日:2015-01-06

    申请号:US14082406

    申请日:2013-11-18

    CPC classification number: C07D209/54

    Abstract: The present invention relates generally to an improved process for the preparation of 5-azaspiro[2.4]heptane-6-carboxylic acid and its derivatives which are useful intermediates in the synthesis of biologically active molecules, especially in the synthesis of hepatits C virus NS5A inhibitors. In particular, the present invention relates to processes and intermediates for the preparation of compounds of formulae (Ia), (Ib) and (Ic):

    Abstract translation: 本发明一般涉及一种制备5-氮杂螺[2.4]庚烷-6-羧酸及其衍生物的改进方法,其在合成生物活性分子中是有用的中间体,特别是在合成肝素C病毒NS5A抑制剂 。 特别地,本发明涉及制备式(Ia),(Ib)和(Ic)化合物的方法和中间体:

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