Stevens Rebecca, Palmer Harry E P, Miah Afjal H, Burley Glenn A
Modality Platform Technologies, GSK, Stevenage SG1 2NY, U.K.
Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow G1 1BX, U.K.
J Org Chem. 2025 Feb 14;90(6):2192-2200. doi: 10.1021/acs.joc.4c02456. Epub 2025 Feb 2.
Ultra high-throughput chemistry carried out in 1536-well plates is increasingly utilized for reaction optimization protocols and direct-to-biology (D2B) platforms, where nanomolar quantities of the final product are directly assessed for biochemical or cellular activity without purification. As their popularity increases, it is crucial that the synthesis of these molecules is reliable and reproducible. Research in our laboratories has identified several nuances of amide couplings when performed on the nanoscale that result in poor translation from 1536-well plates to batch-scale reactions. This case study presents a nanoscale amide coupling reaction to synthesize 700 PROTAC molecules, which identified a range of factors crucial to reaction success on the nanoscale, despite having no influence on reaction conversion in batch. This work presents a guide for high-throughput chemists to consider when working in 1536-well plates and their importance in drawing conclusions from nanoscale synthesis.
在1536孔板中进行的超高通量化学越来越多地用于反应优化方案和直接应用于生物学(D2B)平台,在这些平台中,无需纯化即可直接评估纳摩尔量的最终产物的生化或细胞活性。随着它们越来越受欢迎,这些分子的合成可靠且可重复至关重要。我们实验室的研究发现,在纳米尺度上进行酰胺偶联时存在一些细微差别,这导致从1536孔板到批量反应的转化率较低。本案例研究展示了一个用于合成700种PROTAC分子的纳米尺度酰胺偶联反应,该反应确定了一系列对纳米尺度反应成功至关重要的因素,尽管这些因素对批量反应的转化率没有影响。这项工作为高通量化学家在使用1536孔板工作时提供了一个指南,以及它们在从纳米尺度合成得出结论方面的重要性。