Facile one-pot green synthesis, antioxidant and antimicrobial activities of 7-(substituted phenyl)-7,11-dihydro-6H,8H-chromeno[3′,4′:5,6]pyrano[2,3-d]pyrimidine-6,8,10(9H)-trione derivatives

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Omkar Reddy Vanukuri , Mohan Gundluru , Poojitha Bellala , Rama Sekhara Reddy Dachuru , Suresh Reddy Cirandur
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引用次数: 0

Abstract

The work aims to develop a simple and efficient protocol for one-pot three-component synthesis to produce a series of poly functionalized 7-(substituted phenyl)-7,11-dihydro-6H,8H-chromeno[3′,4′:5,6]pyrano[2,3-d]pyrimidine-6,8,10(9H)-trione derivatives using Sulfonated reduced graphene oxide (rGO-SO3H) as an efficient catalyst via one-pot multicomponent reaction of 4-hydroxycoumarin, aromatic aldehydes and barbituric acid under microwave irradiation and solvent-free conditions in good to excellent yields. The reported protocol is metal-free, highly atom-economic, better yielding in quick reaction time, simple to operate and eco-friendly with reaction conditions comparatively milder. Use of low-cost acidic catalyst under neat conditions makes the reaction an environmentally benign protocol. Additionally, the compounds were screened for their free radical scavenging, antibacterial and antifungal activities which showed good activities when compared than that of standard drugs.
7-(取代苯基)-7,11-二氢- 6h,8H-chromeno[3 ',4 ':5,6]吡喃[2,3-d]嘧啶-6,8,10(9H)-三酮衍生物的抗氧化和抗菌活性
本研究旨在通过4-羟基香豆素的一锅多组分反应,以磺化还原氧化石墨烯(rGO-SO3H)为高效催化剂,建立一种简单高效的一锅三组分合成方案,制备一系列多功能化7-(取代苯基)-7,11-二氢- 6h, 8h -色氨酸[3 ',4 ':5,6]吡喃[2,3-d]嘧啶-6,8,10(9H)-三酮衍生物。芳香族醛和巴比妥酸在微波辐照和无溶剂条件下收率好至优异。该工艺无金属、原子经济性高、反应时间短、操作简单、环境友好,反应条件相对温和。在整洁的条件下使用低成本的酸性催化剂使反应成为一种环境友好的方案。此外,对化合物进行了自由基清除、抗菌和抗真菌活性的筛选,与标准药物相比,显示出较好的活性。
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
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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