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l-Proline Catalyzed Synthesis of Highly Functionalized 4-Hydroxy-4H-chromene-pyrazoles and 4-Hydroxy-4Hchromene-barbiturates in Aqueous Medium

机译:高度功能化的4-羟基-4H-Chromene-吡唑和4-羟基-4HCHROMENE-BARBITURES的L-丙烯催化的合成

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摘要

A simple and efficient method for the synthesis of novel 4-hydroxy-4H-chromene-pyrazoles and 4-hydroxy-4H-chromenebarbiturates was developed from the reaction of 2-ethoxy-2Hchromene chalcones with pyrazolin-5-one and barbituric acid catalyzed by l-proline in water.The developed protocol is applicable for the construction of biologically important 4Hchromenes from easily accessible chalcones having various substituents.This reaction proceeds through Aldol condensation,Michael addition and hydrolysis reactions followed by the elimination of ethoxy group.This methodology offers cleaner conversion,a shorter reaction time and high yields.For the first time,we report the synthesis of novel 4-hydroxy-4H-chromenes from 2-ethoxy-2H-chromene chalcones and pyrazolin-5-one/barbituric acid using l-proline(72–86% yield in 6h).Water was used as the solvent for all the compounds it represents a green synthetic protocol.
机译:一种简单有效的方法,用于合成新型4-羟基-4H-Chromene-吡唑和4-羟基-4H-4H-ChromeneBarbitares,从2-乙氧基-2HCHALCONE与吡唑啉-5-烯丙基酸和巴比妥酸催化的2-乙氧基-2HCHALCONE的反应中开发出来 开发的协议适用于从具有各种取代基的易于访问的墨西哥酮中构建生物学上重要的4HCHROMENES。这种反应通过醛缩合,迈克尔添加和水解反应进行,然后消除乙氧基,这些方法可提供乙氧基含量。 转换,较短的反应时间和高产量。我们首次报告了使用L-丙酸酯和吡唑蛋白-5-一种/巴比妥酸从2-乙氧基-2H-Chromene Chalcones中的新型4-羟基-4H-chromenes合成 (6H的产量为72–86%)。水被用作所有化合物代表绿色合成方案的溶剂。

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