Convergent process for the preparation of a morpholine compound
    2.
    发明授权
    Convergent process for the preparation of a morpholine compound 失效
    用于制备吗啉化合物的收敛过程

    公开(公告)号:US6051717A

    公开(公告)日:2000-04-18

    申请号:US428783

    申请日:1999-10-28

    IPC分类号: C07D249/04 C07D413/06

    CPC分类号: C07D413/06

    摘要: The present invention is directed to the compound 4-N,N-dimethylaminomethyl-5-formyl-1,2,3-triazole which is a valuable intermediate in the preparation of phamaceutical compounds. The present invention is further directed to a novel convergent process for the preparation of 2-(R)-(1-(R)-(3,5-bis(trifluoromethyl)phenyl)-ethoxy)-4-(5-(dimethylamino)methyl-1,2,3-triazol-4-yl)methyl-3-(S)-(4-fluorophenyl)-morpholine which is a potent and selective substance P (or neurokinin-1) receptor antagonist useful as a therapeutic agent.

    摘要翻译: 本发明涉及化合物4-N,N-二甲基氨基甲基-5-甲酰基-1,2,3-三唑,其是制备药物化合物的有价值的中间体。 本发明进一步涉及一种制备2-(R) - (1-(R) - (3,5-双(三氟甲基)苯基) - 乙氧基)-4-(5-(二甲基氨基 )甲基-3-(S) - (4-氟苯基) - 吗啉,其是用作治疗剂的有效和选择性物质P(或神经激肽-1)受体拮抗剂 代理商

    Linear process for the preparation of a morpholine compound
    3.
    发明授权
    Linear process for the preparation of a morpholine compound 失效
    用于制备吗啉化合物的线性方法

    公开(公告)号:US6051707A

    公开(公告)日:2000-04-18

    申请号:US428315

    申请日:1999-10-28

    摘要: The present invention is concerned with a novel linear process for the preparation of 2-(R)-(1-(R)-(3,5-bis(trifluoromethyl) phenyl)-ethoxy)-4-(5-(dimethylamino)methyl-1,2,3-triazol-4-yl)methyl-3-(S)-(4-fluorophenyl)-morpholine which is a potent and selective substance P (or neurokinin-1) receptor antagonist usefull as a therapeutic agent.

    摘要翻译: 本发明涉及制备2-(R) - (1-(R) - (3,5-双(三氟甲基)苯基) - 乙氧基)-4-(5-(二甲基氨基) 甲基-1,2,3-三唑-4-基)甲基-3-(S) - (4-氟苯基) - 吗啉,它是一种有效和选择性物质P(或神经激肽-1)受体拮抗剂,可用作治疗剂 。

    Process for making hydroisoindoline tachykinin receptor antagonists
    6.
    发明授权
    Process for making hydroisoindoline tachykinin receptor antagonists 失效
    制备水解异吲哚啉速激肽受体拮抗剂的方法

    公开(公告)号:US07544815B2

    公开(公告)日:2009-06-09

    申请号:US11484208

    申请日:2006-07-11

    IPC分类号: C07D209/44

    CPC分类号: C07D209/44

    摘要: The present invention is directed to a process for preparing certain hydroisoindoline compounds which are useful as neurokinin-1 (NK-1) receptor antagonists, and inhibitors of tachykinin and in particular substance P. The compounds are useful in the treatment of certain disorders, including emesis, urinary incontinence, depression, and anxiety.

    摘要翻译: 本发明涉及一种制备某些可用作神经激肽-1(NK-1)受体拮抗剂,速激肽抑制剂,特别是物质P的水解异吲哚啉化合物的方法。该化合物可用于治疗某些疾病,包括 呕吐,尿失禁,抑郁和焦虑。

    Process for making hydroisoindoline tachykinin receptor antagonists
    7.
    发明申请
    Process for making hydroisoindoline tachykinin receptor antagonists 失效
    制备水解异吲哚啉速激肽受体拮抗剂的方法

    公开(公告)号:US20070015923A1

    公开(公告)日:2007-01-18

    申请号:US11484208

    申请日:2006-07-11

    IPC分类号: C07D209/44

    CPC分类号: C07D209/44

    摘要: The present invention is directed to a process for preparing certain hydroisoindoline compounds which are useful as neurokinin-1 (NK-1) receptor antagonists, and inhibitors of tachykinin and in particular substance P. The compounds are useful in the treatment of certain disorders, including emesis, urinary incontinence, depression, and anxiety.

    摘要翻译: 本发明涉及制备某些可用作神经激肽-1(NK-1)受体拮抗剂,速激肽抑制剂,特别是物质P的水解异吲哚啉化合物的方法。该化合物可用于治疗某些疾病,包括 呕吐,尿失禁,抑郁和焦虑。