A series of new N-(4-phenyl-1, 3-thiazol-2-yl) benzamides (5a-o) has been synthesized from 2-amino-4-substituted phenylthiazoles and substituted benzoyl chlorides. The structures of synthesized compounds were established based on spectral (FT IR, 1H NMR, ESI Mass) analysis. The final fifteen compounds were screened for anti-inflammatory activity by following carrageenan induced rat paw edema method. Among the compounds screened, N-(4-phenyl-1, 3-thiazol-2-yl) 4-chlorobenzamide (5c) and N-[4-(3-chlorophenyl)-1, 3-thiazol-2-yl]-3-trifluro methylbenzamide (5n) were found to be more potent.
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