Efficient Green Synthesis of Imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole Derivatives Using HPA-Montmorillonite-KSF

Abstract Herein, we developed a simple, efficient, cost-effective, recyclable, and green approach for synthesizing imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole derivatives. The reaction protocol involves ‘HPA-montmorillonite-KSF’ as a reusable and heterogeneous catalyst and proceeds via multicomponent reaction (MCR). Various substituted imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole derivatives were prepared in good to excellent isolated yields. This methodology is compatible with the gram-scale synthesis and provides an efficient and much improved modification of the original MCR, considering the yield and mild reaction conditions.

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Publication Details

Journal
Synlett
Published
2025-04-07
DOI
https://doi.org/10.1055/a-2577-2065
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Efficient Green Synthesis of Imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole Derivatives Using HPA-Montmorillonite-KSF

Danish Khan, Pragati Kushwaha, Manish Gupta, Ayush Bhardwaj
Synlett
Synthesis and biological activity
article

Efficient Green Synthesis of Imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole Derivatives Using HPA-Montmorillonite-KSF

Danish Khan, Pragati Kushwaha, Manish Gupta, Ayush Bhardwaj
article en

Abstract

Abstract Herein, we developed a simple, efficient, cost-effective, recyclable, and green approach for synthesizing imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole derivatives. The reaction protocol involves ‘HPA-montmorillonite-KSF’ as a reusable and heterogeneous catalyst and proceeds via multicomponent reaction (MCR). Various substituted imidazo[2,1-b]thiazol-5-yl-2,4-dihydropyrano[2,3-c]pyrazole derivatives were prepared in good to excellent isolated yields. This methodology is compatible with the gram-scale synthesis and provides an efficient and much improved modification of the original MCR, considering the yield and mild reaction conditions.

SynlettVol. 36(15)
Indian Institute of Technology Roorkee (IN), University of Lucknow (IN), Jai Prakash University (IN)
Council of Science and Technology, U.P., Science and Engineering Research Board
Openalex Percentile: Top 95%
Synthesis and biological activity
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