Department of Discovery Chemistry, Merck & Co., Inc., Rahway, NJ 07065, USA.
Department of Analytical Research & Development, Merck & Co., Inc., Rahway, NJ 07065, USA.
SLAS Technol. 2024 Apr;29(2):100126. doi: 10.1016/j.slast.2024.100126. Epub 2024 Feb 28.
High-throughput experimentation (HTE) has become more widely utilized in drug discovery for rapid reaction optimization and generation of large synthetic compound arrays. While this has accelerated medicinal chemistry design, make, test (DMT) iterations, the bottleneck of purification persists, consuming time and resources. Herein we describe a general parallel purification approach based on solid phase extraction (SPE) that provides a more efficient and sustainable workflow producing compound libraries with significantly upgraded purity. This robust, user-friendly workflow is fully automated and integrated with HTE library synthesis, as demonstrated by its application to a diverse parallel library compound array generated via amide-bond coupling in HTE microscale format.
高通量实验(HTE)在药物发现中得到了更广泛的应用,可用于快速反应优化和生成大型合成化合物阵列。虽然这加速了药物化学设计、制造、测试(DMT)的迭代,但纯化的瓶颈仍然存在,消耗时间和资源。本文中,我们描述了一种基于固相萃取(SPE)的通用平行纯化方法,该方法提供了一种更有效和可持续的工作流程,可生成具有显著提高纯度的化合物库。该方法具有强大的用户友好性,完全自动化,并与 HTE 文库合成集成,通过在 HTE 微尺度格式中通过酰胺键偶联生成的多样化平行文库化合物阵列的应用得到了证明。