Synthesis of 2-(1,2,4-oxadiazol-5-yl)-2,3-dihydro-4H-chromen-4-ones

IF 0.4 Q4 CHEMISTRY, ANALYTICAL French-Ukrainian Journal of Chemistry Pub Date : 2020-12-22 DOI:10.17721/fujcv8i2p176-182
Andrii I. Kysil, A. Biitseva, O. Bugera, T. Yegorova, Z. Voitenko
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引用次数: 0

Abstract

Simple and efficient synthesis of 2-(1,2,4-oxadiazol-5-yl)-2,3-dihydro-4H-chromen-4-ones is elaborated. The method relies on CDI-mediated cyclocondensation of substituted 4-oxochromane-2-carboxylic acids and amidoximes. The protocol allows the preparation of 2-oxadiazolylchromanones decorated with two pharmacophores (2,3-dihydro-4H-chromen-4-one and 1,2,4-oxadiazole) that are in high demand in drug discovery.
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2-(1,2,4-恶二唑-5-基)-2,3-二氢- 4h -铬-4-酮的合成
介绍了2-(1,2,4-恶二唑-5-基)-2,3-二氢-4- h -铬-4-酮的简单高效合成方法。该方法依赖于cdi介导的取代4-氧-2-羧酸和偕胺肟的环缩合反应。该方案允许制备两种药物载体(2,3-二氢- 4h -铬-4- 1和1,2,4-恶二唑)修饰的2-恶二唑酮,这两种药物在药物发现中需求量很大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
French-Ukrainian Journal of Chemistry
French-Ukrainian Journal of Chemistry CHEMISTRY, ANALYTICAL-
自引率
0.00%
发文量
13
审稿时长
4 weeks
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