发明名称 Verfahren zur Herstellung von Cephalosporinantibiotica
摘要 <p>Salts of cephalosporin antibiotics of general formula I with the following amines II: trans-1,3-cyclohexanediamines (A) and their 1,4-analogues (B); trans-1,3-cyclohexane-bis-alkyleneamines (C) and their 1,4-analogues (D) in which the alkylene has up to 3C atoms; 1,3-xylene-alpha,alpha'-diamines (E) and their 1,4-analogues (F). where R = 2-thienylmethyl, 2-furylmethyl, phenylmercaptomethyl, benzyl, nitrobenzyl or CF3-phenyl-mercaptomethyl. and R' = acetoxy (cephalosporanic acid) or H (desacetoxy-cephalosporanic acid). Antibiotics of high and prolonged activity i.e. depot forms resulting from the low solubility in water. The usual Na etc. salts are soluble and when injected parenterally are assimilated and excreted in L hrs. so that 4 injections per day are required.</p>
申请公布号 CH506558(A) 申请公布日期 1971.04.30
申请号 CH19680003695 申请日期 1968.03.13
申请人 ELI LILLY AND COMPANY 发明人 HAROLD FLYNN,EDWIN
分类号 C07D501/20;(IPC1-7):C07D99/24 主分类号 C07D501/20
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