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高效合成手性 2-恶唑烷酮作为药物砌块的方法。

Efficient methods for the synthesis of chiral 2-oxazolidinones as pharmaceutical building blocks.

机构信息

Department of Environmental Science, Graduate School of Fisheries and Environmental Sciences, Nagasaki University, Nagasaki, Japan.

出版信息

Chirality. 2022 Jul;34(7):915-924. doi: 10.1002/chir.23452. Epub 2022 Apr 29.

Abstract

Although the wide variety of heterocyclic compounds is common knowledge, chiral 2-oxazolidinones are recognized as some of the most important heterocycles in medicinal chemistry. Many important pharmaceutical molecules have been constructed based on the chiral 2-oxazolidinone backbone. Therefore, the development of even more efficient catalytic methods for the synthesis of chiral 2-oxazolidinones remains a very important pursuit in the field of synthetic organic chemistry. This review summarizes the coupling reactions of epoxides and isocyanates for the preparation of 2-oxazolidinones. Both metal catalysts and organocatalysts promote these reactions. Optically pure 2-oxazolidinones are prepared from optically pure epoxide substrates via these catalytic methods. A synthetic example of a commercially available pharmaceutical compound utilizing this method is also introduced.

摘要

尽管杂环化合物的种类繁多是众所周知的,但手性 2-恶唑烷酮被认为是药物化学中最重要的杂环之一。许多重要的药物分子都是基于手性 2-恶唑烷酮骨架构建的。因此,开发更有效的催化方法来合成手性 2-恶唑烷酮仍然是合成有机化学领域非常重要的追求。本文综述了环氧和异氰酸酯的偶联反应在制备 2-恶唑烷酮中的应用。金属催化剂和有机催化剂都能促进这些反应。通过这些催化方法,可以从光学纯的环氧底物制备得到光学纯的 2-恶唑烷酮。还介绍了利用该方法合成一种商业上可用的药物化合物的实例。

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