首页> 外国专利> NOVEL PROCESS FOR PREPARING FINASTERIDE OF HIGH PURITY WITH EXCELLENT THERAPEUTIC EFFECT ON POSITIVE PROSTATOMEGALY AND MALE-TYPE ALOPECIA

NOVEL PROCESS FOR PREPARING FINASTERIDE OF HIGH PURITY WITH EXCELLENT THERAPEUTIC EFFECT ON POSITIVE PROSTATOMEGALY AND MALE-TYPE ALOPECIA

机译:制备具有高治疗效果的前列腺素和男性型白内障的高纯度菊苣酯的新方法

摘要

PURPOSE: Provided are a process for preparing finasteride with excellent therapeutic effect on positive prostatomegaly and male-type alopecia, and intermediate compounds useful for the preparation of finasteride. CONSTITUTION: The process for preparing finasteride represented by the formula (I) is prepared by the process comprising the steps of: reacting a compound of the formula (II) with 2,2'-dithiobis(benzothiazole) to produce a reactive derivative compound of the formula (III) and then reacting the compound of the formula (III) with t-butylamine or reacting a compound of the formula (IV) with mercapto benzothiazole to produce an intermediate compound of the formula (V); and converting the compound of the formula (V) obtained in the preceding step into an intermediate compound of the formula (VI) and then heating the compound of the formula (VI) in an organic solvent to dehydrogenate.
机译:目的:提供一种对正前列腺肥大和男性型脱发具有优异治疗效果的非那雄胺的制备方法,以及可用于制备非那雄胺的中间体化合物。组成:由式(I)表示的非那雄胺的制备方法包括以下步骤:使式(II)的化合物与2,2'-二硫代双(苯并噻唑)反应,生成一种活性的式(III),然后使式(III)的化合物与叔丁胺反应,或使式(IV)的化合物与巯基苯并噻唑反应,以制备式(V)的中间体化合物;将上一步骤中得到的式(V)化合物转化为式(VI)的中间体化合物,然后在有机溶剂中加热式(VI)的化合物进行脱氢。

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