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Abstract 3‐(2‐Furyl)‐3‐oxopropanitrile reacts with keto and ester‐hydrazonyl chlorides to afford the corresponding acetyl‐ and ester‐pyrazole derivatives. The latter pyrazoles reacted with hydrazine and gave either the pyrazolo[3,4‐d]pyridazines or pyrazolylhydrazides. Treatment of the latter hydrazides with phenylisothiocyanate and with phenylisocyanate resulted in the formation of the pyrazolylthiadiazole and pyrazolyloxadiazole derivatives, respectively.
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Dawood et al. (2006) studied this question.
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