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
Authors
- Papiya Sikdar (ORCID: https://orcid.org/0009-0008-4573-1233)
- Tathagata Choudhuri
- Avik Kumar Bagdi (ORCID: https://orcid.org/0000-0003-3855-1046)
- Sourav Das (ORCID: https://orcid.org/0000-0002-8155-0383)
- Suvam Paul
Institutions
- University of Kalyani (IN)
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
Funders
- Science and Engineering Research Board