首页> 外国专利> Monohydrate and Anhydrate of gaboxadol in their Crystalline forms I and II; Preparation procedure; Pharmaceutical Composition and its use for the treatment of Neurological or Psychiatric Disorders., Sleep Disorders, hearing, premenstrual syndrome.

Monohydrate and Anhydrate of gaboxadol in their Crystalline forms I and II; Preparation procedure; Pharmaceutical Composition and its use for the treatment of Neurological or Psychiatric Disorders., Sleep Disorders, hearing, premenstrual syndrome.

机译:加波沙朵的一水合物和无水物,其结晶形式为I和II;准备程序;药物组合物及其在治疗神经系统疾病或精神疾病,睡眠障碍,听力,经前综合症中的用途。

摘要

Gaboxadol Monohydrate in Crystalline form, where the form I has a Spectrum of x-ray Powder diffraction in Values of 20 Cuka used radiation with a Peak at 115; and form II has a Spectrum of x-ray Powder diffraction in 20 Cuka values using radiation with a Peak to 25,2u00ba.The procedure to prepare the way I comprises Dissolving a Salt addition of gaboxadol acids in water; add sufficient basis to provide a pH of approximately 6.5; and collect the resulting precipitate immediately.The procedure to prepare the form II includes Dissolving a Salt addition of gaboxadol acids in water; add sufficient basis to provide a pH of approximately 6.5; The resulting mixture left to Mature for at least 12 hours; and collect the resulting Solid.
机译:结晶形式的加波沙朵一水合物,其中形式I具有x射线粉末衍射光谱,其值为20 Cuka,所用辐射的峰值为115;形式Ⅱ的X射线粉末衍射光谱的峰值为25,2 u00ba,辐射强度为20 Cuka。制备方式Ⅰ的步骤包括将加波沙朵酸加成盐溶解在水中;添加足够的基础以提供大约6.5的pH值;制备形式II的方法包括将加波沙朵酸加成盐溶解在水中;将加波沙朵酸加成盐。添加足够的基础以提供大约6.5的pH值;所得混合物至少熟化12小时;并收集所得固体。

著录项

  • 公开/公告号CL2005000165A1

    专利类型

  • 公开/公告日2005-11-04

    原文格式PDF

  • 申请/专利权人 LUNDBECK A/S;

    申请/专利号CL2005000165

  • 发明设计人 VINCENT BRETT COOPER;

    申请日2005-01-28

  • 分类号A61K31/4353;A61P25/08;A61P25/14;A61P25/16;A61P25/18;C07D221/00;C07D261/00;C07D498/04;

  • 国家 CL

  • 入库时间 2022-08-21 22:18:19

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