PREPARATION OF CEPHALOSPORIN DERIVATIVE

    公开(公告)号:JPS57114591A

    公开(公告)日:1982-07-16

    申请号:JP10004481

    申请日:1981-06-26

    Abstract: NEW MATERIAL:The cephalosporin derivative of formulaI[R is H or lower alkyl; X is O, S, or NR (R is H, lower alkyl, etc.); Y is H, lower acyloxy, or SR (R is nitrogen-containing 5-membered heterocyclic group which may have lower alkyl substituent group and may contain O or S)]. EXAMPLE:7-[2-(2-Aminothiaxol-4-yl)acetamido]-3-(1,3,4-thiadiazol-2-yl) thiomethyl- 3-cephem-4-carboxylic acid sodium salt. USE:Antimicrobial agent effective to respiratory infectious diseases, purulent diseases, infectious diseases of the urinary tract, puerperal infectious diseases, etc. Does: 5-20mg/kg daily by parenteral administration divided in 3-4 doses. PROCESS:The compound of formulaIis prepared by the dehydrative cyclization reaction of a novel compound of formula II in a solvent in the presence of an acid or a base. The starting compound of formula II can be prepared by reacting a novel compound of formula III (w is halogen) with a compound of formula IV.

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