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6-氨基青霉烷酸衍生物的研究Ⅰ.6-(取代丙烯酰氨)青霉烷酸的合成
引用本文:段廷漢,雷兴翰. 6-氨基青霉烷酸衍生物的研究Ⅰ.6-(取代丙烯酰氨)青霉烷酸的合成[J]. 药学学报, 1965, 12(8): 516-522
作者姓名:段廷漢  雷兴翰
作者单位:南京药学院,化学工业部上海医药工业研究院 进修教师
摘    要:本文报导了22个6-(取代丙烯酰氨)青霉烷酸化合物的合成.这类化合物系以相应的取代丙烯酸,通过混合酸酐或酰氯,在微碱性、低温下,与6APA进行缩合;再以N-乙基六氢吡啶或N,N′-二苄基乙二胺成盐纯化精制.它们的抗菌作用正在筛选中.

收稿时间:1965-02-25

DERIVATIVES OF 6-AMINOPENICILLANIC ACID Ⅰ. SYNTHESIS OF 6-(SUBSTITUTED ACRYLAMIDO) PENICILLANIC ACID
DWAN T''ING-HAN AND LEI HSING-HAN. DERIVATIVES OF 6-AMINOPENICILLANIC ACID Ⅰ. SYNTHESIS OF 6-(SUBSTITUTED ACRYLAMIDO) PENICILLANIC ACID[J]. Acta pharmaceutica Sinica, 1965, 12(8): 516-522
Authors:DWAN T''ING-HAN AND LEI HSING-HAN
Abstract:Twenty-two new derivatives of 6-aminopenicillanic acid have been prepared either by the mixed carboxylic-carbonic anhydride or by the usual acyl chloride method. They were isolated and purified either as their N-ethylpiperidine or as their N, N'-dibenzyl- ethylenediamine salts. Biological evaluations of these derivatives are in progress.
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