Gefapixant Citrate (MK-7264) Sulfonamide Step Speciation Study: Investigation into Precipitation–Dissolution Events during Addition of Chlorosulfonic Acid

溶解 溶解度 降水 质子化 化学 磺酸 稳健性(进化) 组合化学 有机化学 生物化学 基因 物理 离子 气象学
作者
Nelo R. Rivera,Ryan D. Cohen,Si‐Wei Zhang,Zachary E. X. Dance,Holst M. Halsey,Siqing Song,Xiaodong Bu,Mikhail Reibarkh,Hong Ren,Alfred Y. Lee,Darryl Chang,Sachin Lohani
出处
期刊:Organic Process Research & Development [American Chemical Society]
卷期号:27 (2): 286-294 被引量:2
标识
DOI:10.1021/acs.oprd.2c00313
摘要

Sulfonamidation is the pre-penultimate step in the commercial synthesis of gefapixant citrate. Several stress studies were performed during process characterization of this step to ensure process robustness and to mitigate potential upset scenarios. One parameter explored was the slow addition of chlorosulfonic acid (CSA) to form the sulfonic acid intermediate. During the extended addition, an unexpected series of precipitation–dissolution events were observed. To better understand these events and accommodate a CSA tank switch during the reaction, a detailed investigation using a variety of analytical techniques was performed, which revealed the formation of various protonated species of both the diaminopyrimidine starting material and sulfonic acid intermediate with stark differences in their solubility properties. This behavior explained the changes in solubility observed in the reaction system during CSA addition. This detailed speciation study supported the CSA addition procedure that was ultimately adopted for commercial process to ensure operation robustness.
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