摘要

A new series of 2-amino-3-cyano-4-tetrazoloquinolinylpyridine derivatives has been synthesized by the one-pot cyclocondensation reaction of a tetrazolo[1,5-a]quinoline-4-carbaldehyde, malononitrile, a heterocyclic/aromatic methyl ketone and ammonium acetate. All the synthesized compounds were subjected to in vitro antimicrobial screening against a panel of pathogenic strains of bacteria and fungi. Some of the compounds were found to be equipotent or more potent than commercial antibiotics as evident from the results.

  • 出版日期2009