Cns-depressant compositions and method with(4-(10,11-dihydrodibenz(b,f)oxepin-10-yl)-1-piperazinyl)-alkyl-3-alkyl-2-imidazolidinones
    45.
    发明授权
    Cns-depressant compositions and method with(4-(10,11-dihydrodibenz(b,f)oxepin-10-yl)-1-piperazinyl)-alkyl-3-alkyl-2-imidazolidinones 失效
    (4-(10,11-二氢苯并噻唑(B,F)氧素-10-YL)-1-哌嗪基) - 乙基-3-氨基-2-咪唑啉酮的CNS-抑制剂组合物和方法

    公开(公告)号:US3826833A

    公开(公告)日:1974-07-30

    申请号:US34703873

    申请日:1973-04-02

    申请人: CIBA GEIGY CORP

    CPC分类号: C07D313/14 C07D233/32

    摘要: COMPOUNDS OF THE CLASS OF 1-(2- OR 3-(4-(10-11-DIHYDRODIBENZ(B,F)OXEPIN - 10 - YL) - 1 - PIPERAZINYL)ALKYL)-3-ALKYL-2-IMIDAZOLIDINONE, WHICH CAN BE SUBSTITUTED IN 8-POSITION BY CHLORO, METHYL OR METHOXY, AND THE PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS TTHEREOF, HAVE A DEPRESSANT EFFECT ON THE CENTRAL NERVOUS SYSTEM; PHARMACEUTICAL COMPOSITIONS COMPRISING THESE COMPOUNDS AND A METHOD OF PRODUCING A DEPRESSANT EFFECT ON THE CENTRAL NERVOUS SYSTEM OF WARM-BLOODED ANIMALS ARE PROVIDED. AN ILLUSTRATIVE EMBODIMENT IS 1-(3-(4-(8-CHLORO-10,11DIHYDRODIBENZ(B,F)OXEPIN - 10 YL) - 1 - PIPERAZINYL)PROPYL)-3-METHYL-2-IMIDAZOLIDINONE.

    PROCESS FOR PRODUCING TRANS-DIBENZOXENOPYRROLE COMPOUND AND INTERMEDIATE THEREFOR
    49.
    发明申请
    PROCESS FOR PRODUCING TRANS-DIBENZOXENOPYRROLE COMPOUND AND INTERMEDIATE THEREFOR 失效
    生产二苯并恶唑化合物及其中间体的方法

    公开(公告)号:US20110046393A1

    公开(公告)日:2011-02-24

    申请号:US12667654

    申请日:2008-07-07

    IPC分类号: C07D491/04 C07D313/14

    CPC分类号: C07D313/14 C07D491/044

    摘要: The invention provides a process for production of trans-dibenzoxenopyrrole compounds, in which reduction, leaving group conversion, hydrogenation and methylation are carried out in that order. The process of the invention allows trans-dibenzoxenopyrrole compounds to be produced by a simpler procedure than conventional processes. The invention further provides novel compounds obtained as intermediates in the process, and a process for their production.

    摘要翻译: 本发明提供了生产反式二苯并恶唑并吡咯化合物的方法,其中按顺序进行还原,离去基团转化,氢化和甲基化。 本发明的方法允许通过比常规方法更简单的方法制备反式二苯并恶唑并吡咯化合物。 本发明还提供了在该方法中作为中间体获得的新化合物及其制备方法。