发明名称 CEPHALOSPORINS
摘要 <p>NEW MATERIAL:A compound of formula I [Y is (protected) amino, carboxyl; R1 is 1-6C alkyl, formula II (R3, R4 are H, 1-4C alkyl); R2 is H, protecting group; X is H, halogen, 1-4C alkyl, methylene having 1-4C alkoxy group, substituted nitrogen, methylene substituted with a hetercycle containing 1-4 hetero atoms selected from S and O, formula III (Het is 1-4C alkyl, amino, 5-membered ring containing 1-4 heteroatoms selected from N, S and O)]. EXAMPLE:{ 7-[ 4-( 2-Amino-2-carboxyethyl )-2-imidazolyl ]methoxyiminoaceto }amide-3-acetoxymethyl-3-cephem-4-carboxylic acid. USE:An antibacterial which can be orally administered. PREPARATION:For example, the compound is synthesized according to the process flow shown in the reaction equations (tBu represents tertiary butyl; Boc, tertiary-butoxycarbonyl; Me, methyl; TEA, triethylamine and TFA, trifluoracetic acid).</p>
申请公布号 JPS60130591(A) 申请公布日期 1985.07.12
申请号 JP19830238770 申请日期 1983.12.20
申请人 ASAHI KASEI KOGYO KK 发明人 KUBO KAZUSUKE;KODAMA EIJI;NISHIKIDO JIYOUJI
分类号 C07D501/20;A61K31/545;A61K31/546;A61P31/04;C07D501/59 主分类号 C07D501/20
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