Abstrato

Synthesis, Characterization and Antimicrobial Evaluation of New 5-Acetamido-3-acetyl-1,3,4-oxadiazoline

Hany M. Dalloul and Kholoud Abu Yunis

A new series of 5-acetamido-3-acetyl-1,3,4-oxadiazoline derivatives were synthesized via oxidative cyclization reaction of different N-carbamoyl hydrazones with acetic anhydride. The structures of obtained compounds were confirmed by IR, MS, 1H NMR, 13C NMR and Elemental analysis methods and are in full agreement with their molecular structure. The synthesized 1,3,4-oxadiazolines were screened for in vitro for their biological activity against a variety of bacterial strains (Enterococci, Escherichia coli, Staphylococcus aureus, Klebsiella spp, Proteus spp), and fungi (Aspergillus niger, Candida albicans), employing the nutrient agar disc diffusion method. The obtained results showed that these compounds have good inhibition against the tested pathogens.