Reaction of 2‐dimethylaminomethylene‐1,3‐diones with dinucleophiles. I. Synthesis of 1,5‐disubstituted 4‐acylpyrazoles

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Abstract

Reaction of open‐chain and cyclic sym‐1,3‐diones with N,N‐dimethylformamide dimethyl acetal gave, generally in high yield, a series of sym‐2‐dimethylaminomethylene‐1,3‐diones which reacted with phenylhydrazine and methylhydrazine to afford, generally in satisfactory yield, a number of 1,5‐disubstituted 4‐acylpyrazoles. The applications and limits of this new pyrazole synthesis are presented and discussed. Copyright © 1982 Journal of Heterocyclic Chemistry

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Schenone, P., Mosti, L., & Menozzi, G. (1982). Reaction of 2‐dimethylaminomethylene‐1,3‐diones with dinucleophiles. I. Synthesis of 1,5‐disubstituted 4‐acylpyrazoles. Journal of Heterocyclic Chemistry, 19(6), 1355–1361. https://doi.org/10.1002/jhet.5570190620

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