Preparation of the HIV Attachment Inhibitor BMS-663068. Part 2. Strategic Selections in the Transition from an Enabling Route to a Commercial Synthesis

Author:

Chen Ke1,Risatti Christina1,Simpson James1,Soumeillant Maxime1,Soltani Michelle1,Bultman Michael1,Zheng Bin1ORCID,Mudryk Boguslaw1,Tripp Jonathan C.1,La Cruz Thomas E.1ORCID,Hsiao Yi1,Conlon David A.1,Eastgate Martin D.1ORCID

Affiliation:

1. Chemical & Synthetic Development, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, New Jersey 08903, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference29 articles.

1. aWang, T.; Zhang, Z.; Meanwell, N. A.; Kadow, J. F.; Yin, Z.; Xue, Q. M.; Reguerio-Ren, A.; Matiskella, J. D.; Ueda, Y.; US 2004/011075.

2. bUeda, Y.; Connolly, T. P.; Kadow, J. F.; Meanwell, N. A.; Wang, T.; Chen, C-P. H.; Yeung, K.S.; Zhang, Z.; Leahy, D. K.; Pack, S. K.; Soundararajan, N.; Sirard, P.; Levesque, K.; Thoraval, D.US 2005/0209246, 2005.

3. https://www.viivhealthcare.com/our-medicines/medicines-in-development.aspx.

4. Synthesis of the 6-Azaindole Containing HIV-1 Attachment Inhibitor Pro-Drug, BMS-663068

5. bEastgate, M. D.; Bultman, M. S.; Chen, K.; 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.US2013/0203992, 2013.

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