B.Shah, R.C.Khunt, M.K.Shah
Abstract
Thiazolidin-4-ones (3a-g) have been synthesized by the cyclocondesation at thioglycalic acid with N-aryl-2-chloro- 6-iodo quinonin-3-yl azomethine (2a-g) which in turn have prepared by the action of amines on 2-chloro-6-iodoquinoline- 3-charboxaldihyde1. The structure of the compound (2) and (3) have been confirmed from elemental analysis, further supported by IR, 1H NMR andMass Spectral data.All the products have been screened formtheir antimicrobial activity against severalmicrobe.