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

Abstract

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-Δ2-imidazolin-5-ones, obtained by the reaction

of 1N-amino-2-phenyl-4-arylidene-Δ2-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.