Development of a Large-Scale Route to Glecaprevir: Synthesis of the Side Chain and Final Assembly

被引:13
作者
Hill, David R. [1 ]
Abrahamson, Michael J. [2 ]
Lukin, Kirill A. [1 ]
Towne, Timothy B. [1 ]
Engstrom, Kenneth M. [1 ]
Reddy, Rajarathnam E. [2 ]
Kielbus, Angelica B. [2 ]
Pelc, Matthew J. [1 ]
Mei, Jianzhang [1 ]
Nere, Nandkishor K. [1 ]
Chen, Shuang [1 ]
Henry, Rodger [1 ]
Chemburkar, Sanjay [2 ]
Ding, Chen [3 ]
Zhang, Hongqiang [3 ]
Cink, Russell D. [1 ]
机构
[1] AbbVie Inc, Proc Res & Dev, N Chicago, IL 60064 USA
[2] AbbVie Inc, Operat Sci & Technol, N Chicago, IL 60064 USA
[3] AbbVie Inc, Analyt Res & Dev, N Chicago, IL 60064 USA
关键词
glecaprevir; ABT-493; HCV; Knoevenagel; chiral resolution; INHIBITORS; ESTERS;
D O I
10.1021/acs.oprd.0c00245
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The preceding article described the development of the large-scale synthetic route to macrocycle 3 of glecaprevir (1), a potent HCV protease inhibitor. This article describes the development of the synthesis of the difluoromethyl-substituted cyclopropyl amino acid 4, its conversion to the fully elaborated side chain, amino sulfonamide 2, and the subsequent final coupling to form glecaprevir. The synthesis of amino acid 4 consists of four key transformations: (a) formation of the difluoromethyl-substituted cyclopropane ring of (+/-)-diester 15 via Knoevenagel condensation and Corey-Chaykovsky cyclopropanation, (b) diastereoselective hydrolysis of (+/-)-diester 15 to yield (+/-)-monoacid 14a-b, (c) conversion of (+/-)-monoacid 14a-b to (+/-)-amino ester 10 via a Curtius rearrangement, and (d) resolution of (+/-)-amino ester 10 followed by saponification to give the desired (1R,2R)-amino acid 4. The large-scale synthetic route to amino acid 4 was successfully used to produce the fully elaborated side chain 2 and ultimately the amount of glecaprevir required to support the late-stage clinical development.
引用
收藏
页码:1393 / 1404
页数:12
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