首页> 外国专利> TRIMETYLSILYLOXIKARBONYL-7-AMINODECEFALOSPORANSYRA TRIMETYLSILYLESTER Før ANVAENDNING as an intermediate OCH FOERFARANDE Før FRAMSTAELLNING audio denna.

TRIMETYLSILYLOXIKARBONYL-7-AMINODECEFALOSPORANSYRA TRIMETYLSILYLESTER Før ANVAENDNING as an intermediate OCH FOERFARANDE Før FRAMSTAELLNING audio denna.

机译:在用作中间体之前,应先使用三甲基甲硅烷基氧杂羰基-7-氨基癸酸杂芳酸三苯甲基脂基,并在制造前进行操作。

摘要

In the preferred embodiment of the present invention trimethylsilyl 7-trimethylsilyloxycarbonylaminodecephalosporanate was prepared by bubbling dry carbon dioxide into an anhydrous solution of trimethylsilyl 6-trimethylsilylaminodecephalosporanate and found to be a useful intermediate in the production of cefadroxil and cephalexin by its acylation in anhydrous media with the appropriate 2-phenylglycyl chloride hydrochloride. Other cephalosporins are produced by acylation of 7-trimethylsilyloxycarbonylaminoceph-3-em-4-carboxylic acids or esters having a variety of substituents at the 3-position.
机译:在本发明的优选实施方案中,通过将干燥的二氧化碳鼓泡到三甲基甲硅烷基6-三甲基甲硅烷基氨基去头孢菌素的无水溶液中来制备三甲基甲硅烷基7-三甲基甲硅烷基氧羰基氨基去头孢菌素,并且发现它是通过在无水培养基中与头孢羟氨苄酰化来生产头孢羟氨苄和头孢氨苄的有用中间体。适当的2-苯基甘氨酰氯盐酸盐。其他头孢菌素是通过对3-位具有各种取代基的7-三甲基甲硅烷基氧羰基氨基ceph-3-em-4-羧酸或酯进行酰化而制得的。

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