发明名称 FORTIMICIN DERIVATIVE AND ITS PREPARATION
摘要 <p>NEW MATERIAL:Fortimicin derivatives of formula I (Z is amino group-protecting group; R1 is Z, COCH2NHZ; X is halogen). EXAMPLE:Tetra-N-benzyloxycarbonyl-2-chloro-2-deoxy-2-epifortimicin A. USE:Synthetic intermediate of antibiotic: the dehalogenation and removal of, protection readily give the compound of formula IV (R2 is H, COCH2NH2), an antibiotic. PREPARATION:A compound of formula II is halogenated with, e.g., CCl4-triphenylphosphine to give the compound of formula I. Triphenylphosphine dibromide or triphenylphosphine diiodide may be used as another halogenating agent.</p>
申请公布号 JPS5659792(A) 申请公布日期 1981.05.23
申请号 JP19790135883 申请日期 1979.10.23
申请人 KYOWA HAKKO KOGYO KK 发明人 SUAMI TETSUO
分类号 C07H15/224;C07H15/22 主分类号 C07H15/224
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