发明名称 SYNTHESIS OF ASUKAMYCIN
摘要 PURPOSE:To reduce recemization and obtain the titled antibiotic substance useful as an antimicrobial agent in a few steps, by reacting a specific adenine derivative as a starting material with an alanine derivative and treating the resultant product with an acid. CONSTITUTION:2-Chloro-2-(2',3'-O-isopropylidene-5'-O-sulfamoyl-beta-D- -ribofuranoo xyl)adenine expressed by formula I is reacted with a compound expressed by formula II (Boc is tert-butyloxycarbonyl), e.g. tert-butyloxycarbonyl-L-alanine, etc., in the presence of a proton abstracting agent, e.g. cesium carbonate, nor mally in a solvent, e.g. DMF, preferably at -78 - +100 deg.C for 1-20hr to give a compound expressed by formula III, which is then treated with an acid, e.g. trifluoroacetic acid, to afford the aimed compound expressed by formula IV.
申请公布号 JPS62108896(A) 申请公布日期 1987.05.20
申请号 JP19850247391 申请日期 1985.11.05
申请人 RIKAGAKU KENKYUSHO 发明人 ISONO KIYOSHI;UBUKATA MAKOTO
分类号 C07H19/167 主分类号 C07H19/167
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