首页> 外国专利> A METHOD OF MANUFACTURING (3R,4S)-L-(4-FLUOROPHENYL)-3-(3S)-3-(4-FLUOROPHENYL)-3- HYDROXYPROPYL)-4-(4-HYDROXYPHENYL)-2-AZETIDINONE AND ITS INTERMEDIATES

A METHOD OF MANUFACTURING (3R,4S)-L-(4-FLUOROPHENYL)-3-(3S)-3-(4-FLUOROPHENYL)-3- HYDROXYPROPYL)-4-(4-HYDROXYPHENYL)-2-AZETIDINONE AND ITS INTERMEDIATES

机译:制造(3R,4S)-L-(4-氟苯基)-3-[(3S)-3-(4-氟苯基)-3-羟基丙基)]-4-(4-羟基苯基)-2-氮杂环丁酮的方法及其中间体

摘要

A method of manufacturing (3R,4S)-l-(4-fluorophenyl)-3-[(3S)-3-(4-fluorophenyl)-3- hydroxypropyl)]-4-(4-hydroxyphenyl)-2-azetidinone (ezetimibe) of formula I, in which a protected ketone of general formula II, wherein R stands for a protective group, such as benzyloxycarbonyl, tert-butoxycarbonyl, benzhydryl or trityl, is reduced with asymmetrical borane agents in an inert organic solvent in the temperature range of -30 to +40 °C, and finally the obtained protected alcohol of general formula III, wherein R has the same meaning as above, is deprotected by the action of hydro genolytic or acidic agents in an inert organic solvent.
机译:(3R,4S)-1-(4-氟苯基)-3-[(3S)-3-(4-氟苯基)-3-羟丙基)]-4-(4-羟苯基)-2-氮杂环丁酮的制造方法式I的(ezetimibe),其中通式II的被保护的酮,其中R代表保护基,例如苄氧羰基,叔丁氧羰基,二苯甲基或三苯甲基,在惰性有机溶剂中被不对称硼烷试剂还原。在-30至+ 40℃的温度范围内,最后得到的通式Ⅲ的被保护的醇(其中R具有与上述相同的含义)在惰性有机溶剂中通过氢解或酸化剂的作用脱保护。

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