Abstract
A series of 4-(4-substituted benzylideneamino)-5-phenyl-4H-1,2,4-triazole-3-thiols (IVa-e) was obtained by reaction of 4-(amino)-5-phenyl-4H-1,2,4-triazole-3-thiol with aromatic aldehyde in presence of concentrated sulphuric acid. The synthesised compounds were characterized by FT-IR, 1H-NMR and mass spectra data. The compounds (IVa-e) were screened for their antianxiety activity. Among the compounds, IVa and IVe were found to be the most acitive antianxiety compounds.
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