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批量与流锂化-取代 1,3,4-恶二唑:利用流动化学利用不稳定中间体。

Batch Versus Flow Lithiation-Substitution of 1,3,4-Oxadiazoles: Exploitation of Unstable Intermediates Using Flow Chemistry.

机构信息

Institute of Chemical Sciences, Heriot-Watt University, Riccarton, Edinburgh, UK.

出版信息

Chemistry. 2019 Sep 20;25(53):12439-12445. doi: 10.1002/chem.201902917. Epub 2019 Aug 29.

Abstract

1,3,4-Oxadiazoles are a common motif in pharmaceutical chemistry, but few convenient methods for their modification exist. A fast, convenient, high yielding and general α-substitution of 1,3,4-oxadiazoles has been developed using a metalation-electrophilic trapping protocol both in batch and under continuous flow conditions in contradiction to previous reports which suggest that α-metalation of this ring system results in ring fragmentation. In batch, lithiation is accomplished at an industrially convenient temperature, -30 °C, with subsequent trapping giving isolated yields of up to 91 %. Under continuous flow conditions, metalation is carried out at room temperature, and subsequent in flow electrophilic trapping gave up to quantitative isolated yields. Notably, lithiation in batch at room temperature results only in ring fragmentation and we propose that the superior mixing in flow allows interception and exploitation of an unstable intermediate before decomposition can occur.

摘要

1,3,4-恶二唑是药物化学中的常见结构,但对其进行修饰的方法并不多。我们开发了一种快速、方便、高产且通用的 1,3,4-恶二唑α-取代方法,使用金属化-亲电捕获方案,无论是分批还是连续流动条件下,都与之前的报道形成了对比,之前的报道表明该环系的α-金属化会导致环的断裂。在分批反应中,-30°C 的工业上方便的温度下可以实现锂化,随后的捕获得到最高达 91%的分离产率。在连续流动条件下,室温下进行金属化,随后在流动中进行亲电捕获,得到最高定量的分离产率。值得注意的是,室温下分批锂化仅导致环的断裂,我们提出,在流动中更好的混合可以阻止不稳定的中间体分解,并对其进行拦截和利用。

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