Regioselective Synthesis of Pyrazolo[1,5-a]pyridine via TEMPO-Mediated [3 + 2] Annulation–Aromatization of N-Aminopyridines and α,β-Unsaturated Compounds
Author:
Affiliation:
1. Natural Products Research Centre, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, People’s Republic of China
2. University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China
Funder
National Natural Science Foundation of China
Chinese Academy of Sciences
Sichuan Province
Chengdu Institute of Biology, Chinese Academy of Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00035
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2. Discovery of potent colony-stimulating factor 1 receptor inhibitors by replacement of hinge-binder moieties
3. Discovery of Pyridazinone and Pyrazolo[1,5-a]pyridine Inhibitors of C-Terminal Src Kinase
4. eEary, C. T.; Spencer, S.; Crane, Z.; Chando, K.; Asselin, S.; Liu, W.; Welch, M.; Cook, A.; Kolakowski, G. R.; Metealf, A. T.; Moreno, D. A.; Tang, T. P. Process for the Preparation of 6-(2-Hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile. US Patent 0190106438 A1, 2019.
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