Consecutive three-component synthesis of 3-(hetero)aryl-1H-pyrazoles with propynal diethylacetal as a three-carbon building block

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Abstract

A novel consecutive three-component synthesis of 3-(hetero)aryl-1H- pyrazoles via room temperature Sonogashira arylation of propynal diethylacetal used as a propargyl aldehyde synthetic equivalent has been disclosed. The final acetal cleavage-cyclocondensation with hydrazine hydrochloride at 80 °C rapidly furnishes the title compounds in a one-pot fashion. © 2011 by the authors; licensee MDPI, Basel, Switzerland.

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Levi, L., Boersch, C., Gers, C. F., Merkul, E., & Müller, T. J. J. (2011). Consecutive three-component synthesis of 3-(hetero)aryl-1H-pyrazoles with propynal diethylacetal as a three-carbon building block. Molecules, 16(11), 9340–9356. https://doi.org/10.3390/molecules16119340

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