D.P.Bhoot, H.G.Sangani, R.C.Kh
Abstract
The target compounds 1-aryl-2-phenyl-4-[5’-(m,p-dichlorophenyl)-2’-furylidene]-5-oxo-imidazolines (3a-o) have been synthesized by the condensation of 4-oxo-2-phenyl-5-[5’-(m,p-dichlorophenyl)-2’-furylidene]-oxazole (2)with different arylamines in dry pyridine. All the products have been evaluated for their antimicrobial activity towards different strains of bacteria and fungi and antitubercular activity towards Mycobacterium tuberculosis H37 Rv.