Synthesis and Antimicrobial Activity of Some Substituted Azetidine-2-Ones

摘要

The titled derivatives have been synthesized by condensing aryl and aryloxy acetyl chloride in presence of triethyl amine (TEA) with 1N-amino benzal-2-phenyl-4-arylidene-triangle open 2-imidazolin-5-ones,obtained by the reaction of 1N-amino-2-phenyl-4-arylidene-triangle open 2-imidazolin-5-ones with different aromatic aldehydes. The products have been characterised by IR, NMR and elemental analysis and have been screened for their antimicrobial activity.