首页> 外国专利> As intermediates in the preparation of carbapenem antibiotics useful in the S-carbamoyl-2 and tiokarbamoyylifenyyli-2 (R) - (3S, 4S) -3- £ 1 (R) -trialkyylisilyylioksi) ethyl -2-oxo-4-azetidinyl propionate and -tiopropionaattijohdannaiset and Methods their preparation

As intermediates in the preparation of carbapenem antibiotics useful in the S-carbamoyl-2 and tiokarbamoyylifenyyli-2 (R) - (3S, 4S) -3- £ 1 (R) -trialkyylisilyylioksi) ethyl -2-oxo-4-azetidinyl propionate and -tiopropionaattijohdannaiset and Methods their preparation

机译:作为制备碳青霉烯类抗生素的中间体,可用于S-氨基甲酰基2和tiokarbamoyylifenyyli-2(R)-(3S,4S)-3-£1(R)-三烷基甲硅烷基lyylioksi)乙基| -2-氧代-4-氧杂环丁烷基丙酸酯和-tiopropionaattijohdannaiset及其制备方法

摘要

Compounds of formula (I): CHEM [in which: R1 is hydrogen or a hydroxy-protecting group; R2 is alkyl, alkoxy, halogen, optionally substituted phenyl or optionally substituted phenoxy; R3 is optionally substituted pyridyl, optionally substituted quinolyl or phenyl group which has a substituent of formula -CYNR5R6, where Y is oxygen or sulphur, and R5 and R6 are each alkyl, aryl or aralkyl, or R5 and R6 and the nitrogen to which they are attached together form a heterocyclic group; R4 is hydrogen or an amino-protecting group; and Z is sulphur or oxygen]; are valuable intermediates in the preparation of carbapenem compounds and retain a desirable configuration during conversion to such carbapenem compounds.
机译:式(I)的化合物: [其中:R 1为氢或羟基保护基; R 2为烷基,烷氧基,卤素,任选取代的苯基或任选取代的苯氧基; R 3为任选取代的吡啶基,任选取代的喹啉基或苯基,其具有式-CYNR 5 R 6的取代基,其中Y为氧或硫,并且R 5和R 6各自为烷基,芳基或芳烷基,或R 5和R 6与它们连接在一起的氮形成杂环基; R 4为氢或氨基保护基;且Z为硫或氧];在碳青霉烯化合物的制备中,它们是有价值的中间体,并且在转化成此类碳青霉烯化合物的过程中保持了所需的构型。

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