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DOI: 10.1055/a-2508-9681
A Solvent-Free 2-Chloro-1-methylpyridinium Iodide (CMPI)-Mediated Biginelli Reaction for the Construction of 3,4-Dihydropyrimidin-2(1H)-ones/thiones
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Abstract
The Biginelli product dihydropyrimidinones (DHPMs) and their derivatives have enormous biological significance. This article describes the exploration of 2-chloro-1-methylpyridinium iodide (CMPI) reagent for the development of an environmentally safe, solvent-free protocol to construct the functionalized 3,4-dihydropyrimidin-2(1H)-ones/thiones. The protocol involves the three-component condensation reaction of β-keto ester, aldehyde, and urea or thiourea at elevated temperature. The key advantages of the protocol are its capacity to provide both environmental and economic benefits owing to its solvent-free conditions, short reaction times, simple workup, and good to excellent isolated yield of DHPMs.
Keywords
Biginelli reaction - CMPI - 3,4-dihydropyrimidin-2(1H)-ones/thiones (DHPMs) - one-pot condensation - tri-component reactionSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2508-9681.
- Supporting Information
Publication History
Received: 03 October 2024
Accepted after revision: 30 December 2024
Accepted Manuscript online:
30 December 2024
Article published online:
03 February 2025
© 2025. Thieme. All rights reserved
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