A new series of isoxazoles (7a-d), cyanopyridines (8a-d) and pyrimidinthiones (9a-d) have been prepared from chalcones (6a-d) having s-triazine nucleus. These chalcones on cyclisation with hydroxyl amine hydrochloride in the presence of alkali and malononitrile in the presence of ammonium acetate give isoxazoles (7a-d) and cyanopyridines (8a-d) respectively. Chalcones (6a-d) on condensation with thiourea in the presence of alkali give pyrimidinthiones (9a-d). Structures of newly synthesised compounds were established on the basis of their elemental analysis, IR and 1H NMR spectral data.