Preparation of the HIV Attachment Inhibitor BMS-663068. Part 6. Friedel–Crafts Acylation/Hydrolysis and Amidation
Author:
Affiliation:
1. Chemical & 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.7b00133
Reference31 articles.
1. Synthesis of the 6-Azaindole Containing HIV-1 Attachment Inhibitor Pro-Drug, BMS-663068
2. Preparation of the HIV Attachment Inhibitor BMS-663068. Part 2. Strategic Selections in the Transition from an Enabling Route to a Commercial Synthesis
3. Preparation of the HIV Attachment Inhibitor BMS-663068. Part 5. Selective C-7 Bromination of the 6-Azaindole Core
4. Synthetic Process Development of BMS-599793 Including Azaindole Negishi Coupling on Kilogram Scale
5. bWang, T.; Zhang, Z.; Meanwell, N. A.; Kadow, J. F.; Yin, Z.; Xue, Q. M.; Regueiro-Ren, A.; Matiskella, J. D.; Ueda, Y.U.S. Patent A20040186292, 2004.For general references on amidations with CDI, see:
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