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Process for the preparation of syn-aminothiazolyl and syn-amino-oxazolyl derivatives of alkoxyiminoacetic acids

机译:烷氧基亚氨基乙酸的合成氨基噻唑基和合成氨基恶唑基衍生物的制备方法

摘要

A process has been developed for the preparation of compounds of the general formula: IMAGE where R stands for hydrogen or a lower alkyl, acetyl, beta , beta , beta -trichloroethylcarbonyl, choroacetyl or trityl radical, R1 denotes a lower alkyl radical, R2 denotes hydrogen or a lower alkyl radical and X stands for sulphur or oxygen; as the organic phase, where the alkylation takes place, halogenated hydrocarbons, esters of lower fatty acids, benzene etc. are employed. The aqueous phase, which is mixed with the organic phase, is a 10-50% strength aqueous solution of an inorganic base. The syn-aminothiazolyl and syn-aminooxazolyl derivatives of the alkoxyiminoacetic acids obtained are used as intermediates for the preparation of lactam antibiotics.
机译:已经开发了制备通式化合物的方法:其中R代表氢或低级烷基,乙酰基,β,β,β-三氯乙基羰基,氯代乙酰基或三苯甲基,R1表示低级烷基, R 2表示氢或低级烷基,X表示硫或氧;作为发生烷基化的有机相,使用卤代烃,低级脂肪酸的酯,苯等。与有机相混合的水相是无机碱的10-50%浓度的水溶液。所获得的烷氧基亚氨基乙酸的顺氨基噻唑基和顺氨基恶唑基衍生物用作制备内酰胺抗生素的中间体。

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