Preparation of the HIV Attachment Inhibitor BMS-663068. Part 5. Selective C-7 Bromination of the 6-Azaindole Core
Author:
Affiliation:
1. Chemical and Synthetic Development, Bristol-Myers Squibb Company, One Squibb Drive, New Brunswick, New Jersey 08903-0191, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.7b00132
Reference48 articles.
1. Synthesis of the 6-Azaindole Containing HIV-1 Attachment Inhibitor Pro-Drug, BMS-663068
2. bEastgate, M. D.; Bultman, M. S.; Chen, K. C.; Fanfair, D. D.; Fox, R. J.; La Cruz, T. E.; Mudryk, B. M.; Risatti, C. A.; Simpson, J. H.; Soumeillant, M. C.; Tripp, J. C.; Xiao, Y.Methods for the Preparation of HIV Attachment Inhibitor Piperazine Prodrug Compound. U.S. Patent 2013/0203992.
3. Site-Selective Azaindole Arylation at the Azine and Azole Rings via N-Oxide Activation
4. Recent trends in the chemistry of pyridine N-oxide
5. A Simple and Efficient Method for the Preparation of Pyridine N-Oxides
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