首页> 外国专利> Preparation of citalopram as antidepressant drug and for treating dementia and cerebrovascular disorders comprises reaction of a new intermediate with 3-(N,N-dimethylamino)propyl magnesium halide

Preparation of citalopram as antidepressant drug and for treating dementia and cerebrovascular disorders comprises reaction of a new intermediate with 3-(N,N-dimethylamino)propyl magnesium halide

机译:制备西酞普兰作为抗抑郁药和治疗痴呆和脑血管疾病的方法包括将新中间体与3-(N,N-二甲基氨基)丙基卤化镁反应

摘要

Preparation of citalopram (I) comprises reacting a diphenylketone derivative (IV) with 3-(N,N-dimethylamino)propyl magnesium halide preferably 3-(N,N-dimethylamine)-propyl magnesium chloride and isolating (I) as the base or its salt. Preparation of citalopram of formula (I) comprises reacting a diphenylketone derivative of formula (IV) with 3-(N,N-dimethylamino)propyl magnesium halide preferably 3-(N,N-dimethylamine)-propyl magnesium chloride and isolating (I) as the base or its salt. [Image] R : 1-6C alkyl, 1-6C alkylsulfonyl or arylsulfonyl. Independent claims are included for the following: (1) preparation of a racemic compound of formula (III) which comprises deprotecting (IV) and reacting the obtained compound of formula (VIII) with 3-(N,N-dimethylamino)propyl magnesium halide, preferably 3-(N,N-dimethylamine)-propyl magnesium chloride and (2) new compounds (IV). [Image] ACTIVITY : Antidepressant; nootropic. MECHANISM OF ACTION : Serotonin (5-hydroxytryptamine; 5-HT) reuptake inhibitor.
机译:西酞普兰(I)的制备包括使二苯甲酮衍生物(IV)与3-(N,N-二甲基氨基)丙基卤化镁,优选3-(N,N-二甲基胺)-丙基氯化镁反应并分离(I)作为碱或它的盐。式(I)的西酞普兰的制备包括使式(IV)的二苯基酮衍生物与3-(N,N-二甲基氨基)丙基卤化镁,优选3-(N,N-二甲基胺)-丙基氯化镁反应,并分离(I)作为碱或其盐。 [图像] R:1-6C烷基,1-6C烷基磺酰基或芳基磺酰基。包括以下方面的独立权利要求:(1)制备式(III)的外消旋化合物,其包括将(IV)脱保护并使所得的式(VIII)的化合物与3-(N,N-二甲基氨基)丙基卤化镁反应,优选3-(N,N-二甲胺)-丙基氯化镁和(2)新化合物(IV)。活动:抗抑郁药;促智的。作用机理:5-羟色胺(5-羟色胺; 5-HT)再摄取抑制剂。

著录项

  • 公开/公告号FI118765B

    专利类型

  • 公开/公告日2008-03-14

    原文格式PDF

  • 申请/专利权人 H. LUNDBECK A/S;

    申请/专利号FI20010001316

  • 申请日2001-06-20

  • 分类号C07D307/87;C07C255/56;

  • 国家 FI

  • 入库时间 2022-08-21 20:08:10

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