Rapid Development and Scale-Up of a 1 H -4-Substituted Imidazole Intermediate Enabled by Chemistry in Continuous Plug Flow Reactors

作者
Scott A. May,Martin D. Johnson,Timothy M. Braden,Joel R. Calvin,Brian D. Haeberle,Amy R. Jines,Richard D. Miller,Edward F. Plocharczyk,Gregory A. Rener,Rachel N. Richey,Christopher R. Schmid,Radhe K. Vaid,Hannah Yu
出处
期刊:Organic Process Research & Development [American Chemical Society]
卷期号:16 (5): 982-1002 被引量:76
标识
DOI:10.1021/op200351g
摘要

The development of reactions in a continuous fashion in plug flow tube reactors (PFR) offers unique advantages to the drug development and scale-up process and can also enable chemistry that would be difficult to perform via batch processing. Herein, we report the development of two different continuous flow approaches to a key 1 H -4-substituted imidazole intermediate ( 5 ). In a first generation approach, rapid optimization and scale-up of a challenging cyclization reaction was demonstrated in a PFR under GMP conditions to afford 29 kg of protected product 2 . This material was further processed in batch equipment to deliver di-HCl salt 4 . This first generation approach highlights the rapid development of chemistry in research-scale PFRs and speed to material delivery through linear scale up to a pilot-scale PFR under GMP conditions. In a second generation effort, a more efficient synthetic route was developed, and PFRs with automated sampling, dilution, and analytical analysis allowed for rapid and data-rich reaction optimization of both a key cyclization reaction and thermal removal of a Boc protecting group. This work culminated in 1 kg demonstration runs in a 0.22 L PFR for both continuous steps and shows the potential of commercialization from a lab hood footprint (1–2 MT/year).

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