M. Upreti et al., SYNTHESES OF 1,5-BENZOTHIAZEPINES - PART XIX - SYNTHESES OF 10-SUBSTITUTED BENZOPYRANOBENZOTHIAZEPINES AS PROSPECTIVE CARDIOVASCULAR AGENTS, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 36(12), 1997, pp. 1185-1188
stituted-2-chloro-6a,7-dihydro-6H-7-(4-substituted phenyl)-6-phenyl-[1
]benzopyrano[3,4-c] [1,5] benzothiazepines 3a-l have been synthesized
by reacting (E)-6-chloro-3- (4-chloro/methoxybenzylidene) flavanones 2
a, b with 5-substituted-2-aminobenzenethiols 1a-f by reflux heating in
dry toluene containing piperidine (1:1). The products have been teste
d for purity by TLC and microestimation of nitrogen. IR and H-1 NMR an
d mass spectral studies have enabled the assignment of structures. Bio
assay screening of 3e,f,h and i show mild analgesic and anticonvulsant
activity.