V. Dabholkar, S. Mishra
Sep 1, 2006
Citations
0
Influential Citations
5
Citations
Journal
ChemInform
Abstract
5,5-Dimethyl cyclohexane-1,3-dione 1 has been brominated to yield 2-bromo-5,5-dimethyl cyclohexane-1,3-dione 2 which on further reaction with substituted thiocarbamides, carbamides, 2-aminothiophenols, 2-aminophenol, thiocarbohydrazones, thiosemicarbazones and triazoles has furnished 2-substituted imino-5,5-dimethyl-2,3,5,6 -tetrahydro4H-benzothiazol-7-one 3, 2-substituted imino-5,5-dimethyl-2,3,5,6-tetrahydro-4H-benzoxazol-7-one 4, 7-substituted-2,2dimethyl-2,3-dihydro-1H,10H -phenothiazin-4-one 5, 2,2-dimethyl-2,3-dihydro-1H,10H-phenoxazin-4-one 6, Schiff base of 2-hydrazino-6,6-dimethyl-6,7-dihydro-4H,5H-benzo[1,3,4]thiadiazine-8-one 7, Schiff base of 2-amino-6,6-dimethyl-6,7dihydro-4H,5H-benzo[1,3,4] thiadiazin-8-one 8 and 3-substituted alkyl-7,7-dimethyl-7,8-dihydro-5H,6H-1,2,4-triazolo[3,4b][1,3,4]benzothiadiazin-9-one 9 respectively. All the final compounds have been synthesized by microwave irradiation as well as by conventional method.