Recent Advances in the Synthesis of Functionalized Pyrazolo[1,5-a]pyrimidines via C–H Functionalization

Abstract Recent developments in the synthesis of functionalized pyrazolo[1,5-a]pyrimidines through C–H functionalization have been summarized in this account, covering the synthesis of 3-halo, 3-nitro, 3-formyl, 3-acetyl, 3-sulfenyl, 3-selenyl, and 3-thiocyanato pyrazolo[1,5-a]pyrimidines and bis(pyrazolo[1,5-a]pyrimidin-3-yl)methanes. The main focus highlights the utilization of sustainable conditions in designing the protocols. Mechanistic aspects of these protocols have also been discussed in detail. 1 Introduction 2 Discussion 2.1 Synthesis of 3-Halo Pyrazolo[1,5-a]pyrimidines 2.2 Synthesis of 3-Nitro Pyrazolo[1,5-a]pyrimidines 2.3 Synthesis of 3-Formyl Pyrazolo[1,5-a]pyrimidine 2.4 Synthesis of 3-Acetyl Pyrazolo[1,5-a]pyrimidines 2.5 Synthesis of 3-Sulfenyl Pyrazolo[1,5-a]pyrimidines 2.6 Synthesis of 3-Selenyl Pyrazolo[1,5-a]pyrimidines 2.7 Synthesis of 3-Thiocyanated Pyrazolo[1,5-a]pyrimidines 2.8 Synthesis of Bis(pyrazolo[1,5-a]pyrimidinyl)methanes 3 Conclusions and Outcome

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Publication Details

Journal
Synlett
Published
2025-01-27
DOI
https://doi.org/10.1055/a-2526-0771
Citations
7
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
6.55

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article

Recent Advances in the Synthesis of Functionalized Pyrazolo[1,5-a]pyrimidines via C–H Functionalization

Papiya Sikdar, Tathagata Choudhuri, Avik Kumar Bagdi, Sourav Das et al.
7 citations
Synlett
Synthesis and Biological Evaluation
6.55
article

Recent Advances in the Synthesis of Functionalized Pyrazolo[1,5-a]pyrimidines via C–H Functionalization

Papiya Sikdar, Tathagata Choudhuri, Avik Kumar Bagdi, Sourav Das, Suvam Paul
article en
7 citations

Abstract

Abstract Recent developments in the synthesis of functionalized pyrazolo[1,5-a]pyrimidines through C–H functionalization have been summarized in this account, covering the synthesis of 3-halo, 3-nitro, 3-formyl, 3-acetyl, 3-sulfenyl, 3-selenyl, and 3-thiocyanato pyrazolo[1,5-a]pyrimidines and bis(pyrazolo[1,5-a]pyrimidin-3-yl)methanes. The main focus highlights the utilization of sustainable conditions in designing the protocols. Mechanistic aspects of these protocols have also been discussed in detail. 1 Introduction 2 Discussion 2.1 Synthesis of 3-Halo Pyrazolo[1,5-a]pyrimidines 2.2 Synthesis of 3-Nitro Pyrazolo[1,5-a]pyrimidines 2.3 Synthesis of 3-Formyl Pyrazolo[1,5-a]pyrimidine 2.4 Synthesis of 3-Acetyl Pyrazolo[1,5-a]pyrimidines 2.5 Synthesis of 3-Sulfenyl Pyrazolo[1,5-a]pyrimidines 2.6 Synthesis of 3-Selenyl Pyrazolo[1,5-a]pyrimidines 2.7 Synthesis of 3-Thiocyanated Pyrazolo[1,5-a]pyrimidines 2.8 Synthesis of Bis(pyrazolo[1,5-a]pyrimidinyl)methanes 3 Conclusions and Outcome

SynlettVol. 36(10)
University of Kalyani (IN)
Science and Engineering Research Board
Openalex Percentile: Top 4%
Synthesis and Biological Evaluation
6.55
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Recent Advances in the Synthesis of Functionalized Pyrazolo[1,5-a]pyrimidines via C–H Functionalization — Papiya Sikdar, Tathagata Choudhuri, et al. · Synlett (2025) | TGRS Research Map | TGRS