发明名称 CEPHALOSPORIN COMPOUND FOR ORAL ADMINISTRATION
摘要 <p>NEW MATERIAL:A compound (syn isomer) of formulaI[R1 is H or lower alkyl; R2 is lower alkyl; Y is phthalidyl or a group of formula II (R3 is H or CH3; R4 is lower alkyl or lower lakoxyl)]and a pharmacologically acceptable acid addition salt thereof. EXAMPLE:Pivaloyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-methoxymethyl-3- cephem-4-carboxylate. USE:An antimicrobial agent for oral administration, having good absorption from the digestive tracts, and capable of decomposing the ester part at the 4-positin rapidly in the living body to form the carboxylic acid type. PROCESS:A compound of formula III is reacted with a compound of formula IV (R5 is optionally protected NH2; R6 is optionally protected OH or lower alkoxyl) or a reactive derivative thereof, and if necessary the protecting groups are removed to give the compound of formulaI.</p>
申请公布号 JPS5762287(A) 申请公布日期 1982.04.15
申请号 JP19810111440 申请日期 1981.07.16
申请人 SANKYO KK 发明人 NAKAO HIDEO;FUJIMOTO KOUICHI;ISHIHARA SADAO;SUGAWARA SHINICHI;IGARASHI ISAMU
分类号 C07D501/34;A61K31/545;A61K31/546;A61P31/04 主分类号 C07D501/34
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