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Table · dataset · 2026

Mechanochemical Access to 2,4-Diaroyl-5-aminothiazoles from β‑Ketothioamides at Room Temperature

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A mechanochemical approach to hitherto unreported 2,4-diaroyl-5-aminothiazoles via formal [3 + 2] heteroannulation of β-ketothioamides with 3-(hydroxyimino) chromane-2,4-diones has been developed utilizing SiO<sub>2</sub>-assisted hand grinding in a mortar with pestle at room temperature within 10 min.

Description

The reaction proceeds via C(sp<sup>2</sup>)–S bond formation/dehydrative intramolecular cyclization cascade. This strategy is distinguished by safe and easily accessible substrates, metal-free mild conditions, broad substrate scope, and wide functional group compatibility.

Control experiments, DFT, and HRMS studies validated the proposed mechanism.

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figshareoai:figshare.com:article/3388290610 d agoJSON v1
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