Abstract

D. Sreenivasa Rao, E. Jayachandran*, G. M. Sreenivasa and B. Shivakumar

The title compounds are prepared by starting from Fluoro chloro aniline to 2-amino benzothiazole, which is converted further into 2-hydrazino benzothiazoles, then it is treated with para tolyl sulphonyl chloride to obtain N-p-tolyl sulphon hydrazino 6-fluoro-7-chloro (1,3) benzothiazoles. Finally the above said compounds treated with different amines to get derivative compounds. The synthesized compounds are screened for anti-inflammatory activity. Some of these compounds shows promising anti-inflammatory activity.

Inhibition of albumin

[ View HTML Full Text]