R. Khunt et al., Synthesis and biological evaluation of 3-aryl-2-(2-chloro-7-methoxyquinolin-3-yl)-4-thiazolidinones, J INDIAN CH, 78(1), 2001, pp. 47-48
3-Aryl-2-(2-chloro-7-methoxyquinolin-3-yl)-4-thiazolidinones (3a-m, 4a-m) h
ave been synthesised by the condensation of thioglycolic acid/thiolactic ac
id with N-aryl-(2-chloro-7-methoxyquinolin-3-yl)azomethine (2a-m) which in
turn are prepared from arylamine and 2-chloro-7-methoxyquinoline-3-carboxal
dehyde (1). The products have been evaluated for their antibacterial and an
tifungal activities.