Facing chirality in the 21st century: Approaching the challenges in the pharmaceutical industry

被引:59
作者
Federsel, HJ [1 ]
机构
[1] AstraZeneca R&D, Proc R&D, S-15185 Sodertalje, Sweden
关键词
drug development; chiral pharmaceuticals; risk profile; azetidinecarboxylic acid; esomeprazole; enantioselective oxidation; Ti-catalyzed sulfoxidation; chromatographic resolution; triazolo pyrimidines; steroid acetalization;
D O I
10.1002/chir.10274
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
How is process R&D organized and operated in today's pharmaceutical industry at the dawn of the 21st century? A way to respond to the challenges with regard to reduced time to market is to build on early involvement and a front-loading approach. This means that activities are initiated during the lead optimization phase starting up to 2 years ahead of candidate drug nomination and a model built on this concept covering the stages through to commercial launch is advocated as the appropriate way forward. However, given the high attrition rate in a pharma R&D pipeline focused risk management needs to be applied and options judiciously evaluated. From a molecular perspective, the chemical targets in many instances present a formidable complexity both with regard to the overall structure but increasingly also when it comes to their stereochemical features. Thus, a novel triazolo pyrimidine compound with six stereogenic centers requiring 28 transformations for its assembly is examined to underscore this, but also the difficulties in designing a feasible route for the relatively simple (S)-azetidinecarboxylic acid are highlighted. Furthermore, the successful development of a unique and highly efficient catalytic asymmetric sulfide oxidation to the corresponding (S)-sulfoxide esomeprazole is discussed, together with the remarkable effect that normal sea sand has on the stereoselectivity of a steroid trans-acetalization. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:S128 / S142
页数:15
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