Abstract
The reactivity of methyl-2-isothiocyana-tobenzoic acid 2 towards nitrogen nucleophiles
was investigated. When compound 2 was reacted with sulfanilamide and/or sulfacetamide
the thioureido derivatives 3 and 4 were obtained. Refluxing of compound 3 or 4 with
hydrazine hydrate in ethanol afforded the N-amino-quinazoline derivatives 5 and 6,
respectively. When compound 5 was reacted with aromatic aldehydes in ethanol, the
novel Schiff's bases 7–9 were produced. In a similar manner, aromatic aldehyde were
reacted with compound 6 in acetic acid containing fused sodium acetate to furnish
the triazoloquinazoline derivatives 10–13. Also, triazoloquinazoline derivative 14
was obtained via reaction of compound 6 with acetic anhydride. In addition, the corresponding
triazinoquinazoline derivative 16 was obtained vi reaction of compound 6 with ethyl
chloroacetate. The triazoloquinazoline 19 was obtained in good yield via the reaction
of 6 with diethyloxalate. Moreover some of the newly synthesized compounds showed
good antipyretic and anti-inflammatory activities.
Key word
Quinazolines, antipyretic and anti-inflammatory activities - Sulfonamide moiety