Experimental chemical synthesis demonstrates efficient production of 1,3-diaryl-4-methylthio-5-acyl-pyrazoles, suggesting a versatile route for novel heterocyclic compounds.
We herein report the reaction between α-oxodithioesters and methyl ketones in the presence of sodium hydride and methyl iodide in DMF for the synthesis of symmetrical α,β-bis(methylthio)-α,β-unsaturated-1,4-diketones, which are novel key compounds. We explored potential application of these intermediates by reacting with arylhydrazines in the presence of potassium hydroxide in isopropyl alcohol at 75 °C, which afforded 1,3-di(hetaryl/aryl)-4-methylthio-5-acyl-pyrazoles in high yields and short reaction times. Wide substrate scope, development of novel key intermediates and pyrazoles, are the advantages of this protocol
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Prapullachandra et al. (2026) studied this question.
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