发明名称 PROCESS FOR PREPARING CEPHALOSPORIN DERIVATIVES
摘要 <p>Cephalosporin derivs. and salts of formula (I) are prepared. In (I), R1 is ester-bonded-alpha-beta- or gamma-amino acid with NH2 opt. substd. 1 or 2 C1-4 alkyl; R2 is 1-alkanoyloxyalkyl, 1alkoxycarbonyloxyalkyl, phthalidyl, or 5-methyl-1,3-dioxolin-2-on4- methyl; R3 is carbamoyloxymethyl, opt. substd.; R4 is H or OH; pref. D-configuration. (I) are stable sol., readily absorbable cephalosporins for P.O. admin. readily enzymically hydrolyzed in vivo to unesterified deriv. (II), maintained for long periods at high blood conc. and with high antibacterial activity.</p>
申请公布号 KR900007200(B1) 申请公布日期 1990.10.05
申请号 KR19830004949 申请日期 1983.10.20
申请人 KYOTO PHARMACEUTICAL IND.CO.,LTD. 发明人 KAKEYA NOBUHARU;NISHIZAWA SUSUMU;TAMAKI SATOSHI;KITAO KAZUHIKO
分类号 C07D501/36;A61K;A61K31/545;A61K31/546;A61P31/04;B60J10/08;C07D;C07D501/04;C07D501/24;C07D501/32;C07D501/34;C07D501/44;C07D501/46;C07D501/54;(IPC1-7):C07D501/36 主分类号 C07D501/36
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