Perez Gonzalez Eduardo R, Reck Bernhard, Kalaba Predrag, Langer Thierry, Leban Johann, Lubec Gert
Fine Organic Chemistry Lab, School of Sciences and Technology, São Paulo State University (UNESP), Presidente Prudente 19060-080, São Paulo, Brazil.
ChemCon GmbH, 79108 Hamburg, Germany.
ACS Omega. 2024 Mar 4;9(11):12976-12983. doi: 10.1021/acsomega.3c09348. eCollection 2024 Mar 19.
Large-scale syntheses of small molecules and kilo laboratories are crucial steps in drug development, especially in advanced stages. ()-5-((Benzhydrylsulfinyl)methyl)thiazole, ()-CE-123, a potent, selective, and novel atypical DAT inhibitor, has undergone iterative testing as part of the preclinical evaluation step. This required the process transfer, scale-up, and synthesis of a 1 kg preclinical batch. The Kagan protocol for asymmetric sulfide to sulfoxide oxidation was successfully applied within a four-step synthetic process for the successful upscaling of ()-CE-123. During the scale-up of the last step, several changes were made to the original synthetic procedure, as with every increase in batch size, new problems had to be overcome. These include, among others, the workup optimization of the last step, the simplification of chromatographic purification, elution modification to improve the purity of the product and saving of workup time. Two washing steps were added to the original procedure to enhance both the yield and the enantiomeric excess value of the final product. The modifications introduced allowed access to a 1 kg ()-CE-123 batch with a purity >99% and an enantiomeric excess value of 95%.
小分子的大规模合成和公斤级实验室是药物开发中的关键步骤,尤其是在后期阶段。()-5-((二苯甲基亚磺酰基)甲基)噻唑,()-CE-123,一种强效、选择性且新型的非典型多巴胺转运体(DAT)抑制剂,作为临床前评估步骤的一部分,已经历了迭代测试。这需要进行工艺转移、放大以及合成1公斤临床前批次的产品。卡根不对称硫化物到亚砜氧化的方案在()-CE-123成功放大的四步合成过程中得到了成功应用。在最后一步放大过程中,对原始合成程序进行了若干更改,因为随着批次规模的每次增加,都必须克服新的问题。其中包括最后一步的后处理优化、色谱纯化的简化、洗脱改性以提高产品纯度以及节省后处理时间。在原始程序中增加了两个洗涤步骤,以提高最终产品的收率和对映体过量值。所引入的修改使得能够获得纯度>99%且对映体过量值为95%的1公斤()-CE-123批次产品。