Some new imidazolinyl-pyrazoles (4) were synthesized by condensation o
f 2-imidazolylhydrazine hydroiodid (la) with beta-ketoesters to afford
the intermediate 3 that, as free base, ring closes only to 4. The att
empt to obtain the imidazo-triazepinone 5, starting from 2-imidazoliny
l-2-methylhydrazine, was accomplished, in low yield, only in reacting
with ethyl acetoacetate. The pharmacological evaluation of antiinflamm
atory and analgesic activities of pyrazoles 4a-f revealed an appreciab
le antiinflammatory activity.