Advanced Chemistry Technologies Group, AbbVie, Inc., North Chicago, Illinois 60064, United States.
J Org Chem. 2022 Feb 18;87(4):1880-1897. doi: 10.1021/acs.joc.1c01427. Epub 2021 Nov 15.
Parallel library synthesis is an important tool for drug discovery because it enables the synthesis of closely related analogues in parallel via robust and general synthetic transformations. In this perspective, we analyzed the synthetic methodologies used in >5000 parallel libraries representing 15 prevalent synthetic transformations. The library data set contains complex substrates and diverse arrays of building blocks used over the last 14 years at AbbVie. The library synthetic methodologies that have demonstrated robustness and generality with proven success are described along with their substrate scopes. The evolution of the synthetic methodologies for library synthesis over the past decade is discussed. We also highlight that the combination of parallel library synthesis with high-throughput experimentation will continue to facilitate the discovery of library-amenable synthetic methodologies in drug discovery.
平行库合成是药物发现的重要工具,因为它能够通过稳健且通用的合成转化来平行合成密切相关的类似物。在这个视角下,我们分析了超过 5000 个平行库中使用的合成方法,这些库代表了 15 种流行的合成转化。该库数据集包含复杂的底物和过去 14 年 AbbVie 中使用的各种构建块。描述了具有稳健性和通用性且已被证明成功的库合成方法及其底物范围。讨论了过去十年中库合成的合成方法的演变。我们还强调,将平行库合成与高通量实验相结合将继续促进在药物发现中发现适合库的合成方法。