Abstract A compound of the formula ##STR1## wherein A represents acetoxy group, carbamoyloxy group or (1-metyl-1H-tetrazol-5-yl)thio group and Y represents propargylthio group, azidomethylthio group, 2-hydroxyethylthio group, 3-isoxazolyloxy group, 3-isoxazolylthio group, methylsulfonyl group, ethylsulfonyl group, 2-cyanoethyl-sulfonyl group or sydnon-3-yl group and nontoxic pharmaceutically acceptable salts thereof are prepared by a process which comprises reacting a compound of the formula ##STR2## wherein R represents a protective group for a carboxyl group and A has the same meaning as defined above with a carboxylic acid of the formula Y - CH.sub.2 COOH wherein Y has the same meaning as defined above or a reactive derivative thereof to give a compound having the formula ##STR3## wherein A, R and Y have the same meanings as defined above and removing the protective group for the carboxyl group from said compound. The compounds are antibacterial agents.
A compound having the formula ##STR23## wherein A represents a (1-methyl-1H-tetrazol-5-yl)thio group and Y represents a 2-hydroxy-ethylthio group, a methylsulfonyl group, an ethylsulfonyl group, or a sydnon-3-yl group and a nontoxic pharmaceutically acceptable salt thereof.
Claim 2
Dependent Claim
35 words
A compound having the formula ##STR23## wherein A represents a (1-methyl-1H-tetrazol-5-yl)thio group and Y represents a 2-hydroxy-ethylthio group, a methylsulfonyl group, an ethylsulfonyl group, or a sydnon-3-yl group and a nontoxic pharmaceutically acceptable salt thereof.