发明名称 PREPARATION PROCESS OF CEPHALOSPORINS
摘要 <p>Cephalosporins of formula (I) and their pharmaceutically acceptable salts and esters are new (R = organic acylamino, Y = N-contg. 5-membered ring. n = 0 or 1. R1 and R2 are H or 1-6C alkyl. R3 and R4 are each 1-3C alkyl or together they complete a monocyclic ring). Also new are the intermediates of formulae (VI) and (IXA) (where Rx = H or a blocking gp. m = 0 or 1. The dotted line is a double bond at 2 or 3 posn.). Cpds. (I) are antibacterials for use in human or veterinary medicine and are administered in usual oral, topical or parenteral forms e.g. unit doses of 50-500 mg for an adult human dose of 0.1-3 g/day. They are pref. used together with clavulanic acid or its derivs. A typical cpd. is 7- D-alpha-(3-benzoyl-3-methylureido) phenylacetamido -3-(2-carbamoylmethyl-1,3,4-oxadiazol-5-ylthio) methylceph-3-em-4-carboxylic acid/.</p>
申请公布号 GR61821(B) 申请公布日期 1979.01.22
申请号 GR19637601522 申请日期 1976.11.25
申请人 BEECHAM GROUP LTD 发明人
分类号 A61K31/42;A61K31/545;A61K31/546;A61P31/04;C07D249/02;C07D257/04;C07D271/10;C07D271/113;C07D285/12;C07D285/125;C07D501/36;C07D501/58;C07D501/60;(IPC1-7):07D501/36 主分类号 A61K31/42
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