Amorphous and crystalline forms of losartan potassium and process for their preparation
    73.
    发明授权
    Amorphous and crystalline forms of losartan potassium and process for their preparation 失效
    氯沙坦钾的无定形和结晶形式及其制备方法

    公开(公告)号:US07332612B2

    公开(公告)日:2008-02-19

    申请号:US10293820

    申请日:2002-11-13

    IPC分类号: C07D403/10

    CPC分类号: C07D403/10

    摘要: This invention relates to novel amorphous losartan potassium, novel losartan potassium in a crystalline form that is a hydrate, novel crystalline losartan potassium Form IV and solvates thereof, novel crystalline losartan potassium Form V and solvates thereof, to processes for their preparation, to compositions containing them and to their use in medicine. This invention further relates to a novel process for preparing crystalline losartan potassium Form I and Form II.

    摘要翻译: 本发明涉及新型无定形洛沙坦钾,结晶形式的新型氯沙坦钾,其为水合物,新型结晶氯沙坦钾形式IV及其溶剂合物,新型结晶氯沙坦钾V型及其溶剂化物,其制备方法,含有 他们和他们在医学中的使用。 本发明还涉及一种制备结晶氯沙坦钾I型和II型的新方法。

    Crystal forms of oxcarbazepine and processes for their preparation
    77.
    发明授权
    Crystal forms of oxcarbazepine and processes for their preparation 失效
    奥卡西平的晶体形式及其制备方法

    公开(公告)号:US07183272B2

    公开(公告)日:2007-02-27

    申请号:US10074181

    申请日:2002-02-12

    CPC分类号: C07D223/22

    摘要: The present invention provides for new crystal forms of oxcarbazepine, more particularly oxcarbazepine Forms B, C, D and E. The present invention further provides processes for preparation of these forms. Form B is prepared by evaporating the solvents from a solution of oxcarbazepine in toluene and dichloromethane. Form B is also obtained by immediately cooling the solution of oxcarbazepine and toluene. Cooling the same solution at a slower rate, but still fairly rapidly, results in oxcarbazepine Form C. Cooling the same solution at even a slower rate results in another Form, oxcarbazepine Form D. Oxcarbazepine Form E, a solvate of chloroform, is obtained by precipitating a solution of oxcarbazepine and chloroform. The present invention also provides processes for converting one of the newly discovered crystal forms of oxcarbazepine into another crystal form, including Form A, which is in the prior art. These conversions may occur by storage at ambient temperature, by heating one particular Form or treatment with a protic solvent.

    摘要翻译: 本发明提供了奥卡西平,更特别是奥卡西平形式B,C,D和E的新结晶形式。本发明还提供了这些形式的制备方法。 通过从奥卡西平溶于甲苯和二氯甲烷的溶液中蒸发溶剂制备形式B. 通过立即冷却奥卡西平和甲苯的溶液也可获得形式B. 以较慢的速度冷却相同的溶液,但仍然相当快速地导致奥卡西平形式C.以更慢的速率冷却相同的溶液导致另一种形式奥卡西平形式D.奥卡西平E型氯仿溶剂化物通过 沉淀奥卡西平和氯仿溶液。 本发明还提供了将新发现的奥卡西平晶体之一转化为另一种晶体形式的方法,包括现有技术中的形式A. 这些转化可以通过在环境温度下储存,通过加热一种特定形式或用质子溶剂处理来进行。

    Preparation of tadalafil intermediates
    79.
    发明申请
    Preparation of tadalafil intermediates 审中-公开
    他达拉非中间体的制备

    公开(公告)号:US20060276652A1

    公开(公告)日:2006-12-07

    申请号:US11403582

    申请日:2006-04-12

    IPC分类号: C07D471/02

    CPC分类号: C07D471/04

    摘要: Provided is a process for preparing tadalafil intermediates in various solvents. Also provided is a method for converting said intermediates to tadalafil.

    摘要翻译: 提供了在各种溶剂中制备他达拉非中间体的方法。 还提供了将所述中间体转化为他达拉非的方法。