首页> 外文期刊>Monatshefte fur Chemie >One-pot three-component reaction for facile and efficient green synthesis of chromene pyrimidine-2,4-dione derivatives and evaluation of their anti-bacterial activity
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One-pot three-component reaction for facile and efficient green synthesis of chromene pyrimidine-2,4-dione derivatives and evaluation of their anti-bacterial activity

机译:用于体育嘧啶-2,4-二酮衍生物的体育和有效绿色合成的一锅三组分反应及其抗菌活性的评价

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摘要

A facile and highly efficient one-pot three-component synthesis of chromene pyrimidine-2,4-dione derivatives from available substrates catalyzed by heteropoly acid (H3PW12O40) is described. In this protocol, the reaction of diverse aldehydes, 4-hydroxycoumarin, and 4-amino-1,3-dimethyluracil in the mixture of EtOH / H2O (1:2) at room temperature in the presence of heteropoly acid (H3PW12O40) as a highly efficient catalyst affords the corresponding chromene pyrimidine-2,4-dione in good to excellent yields. Operational simplicity, low cost, eco-friendly with the environment, easy workup and purification, short reaction time, high yield of products, green media of the reaction and mild conditions are the advantages of this method. The in vitro antibacterial activities of title compounds were obtained againstEscherichia coli(ATTC 35218) andStaphylococcus aureus(ATCC 6538) as Gram-negative and Gram-positive bacteria, respectively, and their activities were compared to gentamycin and penicillin as reference drugs.
机译:描述了来自杂多酸(H3PW12O40)催化的可用底物的铬丙酰胺-2,4-二酮衍生物的容易和高效的一罐三组分合成。在该方案中,在杂多酸(H3PW12O40)存在下,在室温下,在EtOH / H 2 O(1:2)的混合物中,在室温下在室温下反应。高效的催化剂提供相应的Chromene嘧啶-2,4-二酮,良好至优异的产率。运行简洁,成本低,环保环境,易于余辉,效率短,产品高产量,反应绿色介质和温和条件是该方法的优势。作为革兰氏阴性和革兰氏阳性细菌,获得了标题化合物的体外抗菌活性,分别为革兰氏阴性和革兰氏阳性细菌,将它们的活性与庆大霉素和青霉素作为参考药物进行比较。

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