发明名称 NEW ANTHRACYCLINE DERIVATIVE HAVING 4-AMINO-2,4,6-TRIDEOXY-2-FLUORO-ALPHA-L-TALOPYRANOSYL GROUP
摘要 PROBLEM TO BE SOLVED: To obtain a new daunomycinone or adriamycinone derivative (acid adduct) having an anticancer activity, excellent in water solubility and useful as an antitumor medicine, etc. SOLUTION: A compound of formula I (R is H, hydroxyl). For example, 7-O-(4-amino-2,4,6-trideoxy-2-fluoro-α-L-talopyranosyl)daunomycin. The compound of formula I is obtained e.g. by condensing daunomycinone of formula II with a 3,4-di-O,N-protected-4-amino-2,4,6-trideoxy-2-fluoro-L-talopyranosyl halide of formula III (Y' is acetyl, benzoyl; Y" is trifluoroacetyl; X is bromine, iodine) and subsequently removing the hydroxyl-protecting group and the amino- protecting group from the produced compound of formula IV.
申请公布号 JPH10175992(A) 申请公布日期 1998.06.30
申请号 JP19960335913 申请日期 1996.12.16
申请人 MICROBIAL CHEM RES FOUND 发明人 TAKEUCHI TOMIO;UMEZAWA SUMIO;TSUCHIYA OSAMU;TAKAGI YASUSHI
分类号 C07H5/06;A61K31/70;A61K31/7008;A61K31/7028;A61K31/7034;A61K31/704;A61P35/00;C07H15/12;C07H15/252;(IPC1-7):C07H15/252 主分类号 C07H5/06
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