Green preparation of new pyrimidine triazole derivatives via one-pot multicomponent reactions of guanidine

IF 3.9 2区 化学 Q2 CHEMISTRY, APPLIED
Nasrin Karami Hezarcheshmeh, Farideh Godarzbod, Media Noori Abdullah, Zinatossadat Hossaini
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引用次数: 0

Abstract

In this research the goal was to produce novel pyrimidine triazole compounds in high yields using triethylamin as an efficient catalyst. These new compounds were synthesized by using multicomponent reaction of aldehydes, guanidine, electron deficient acetylenic compounds, tert-butyl isocyanide and hydrazonoyle chloride in aqueous media. Due to the presence of an NH group, which was assessed using two different methodologies, newly synthesized pyrimidine triazoles have antioxidant properties. Additionally, the antibacterial activity of newly created pyrimidine triazoles was assessed using the disk distribution method with two different types of Gram-positive bacteria and Gram-negative bacteria, demonstrating that the use of these compounds prevented the growth of bacteria. Applied to the preparation of pyrimidine triazole derivatives, this method has short reaction times, high product yields, and the ability to separate catalyst and product using simple procedures.

Abstract Image

胍的一锅多组分反应制备新型嘧啶三唑衍生物。
在这项研究中,目标是使用三乙基胺作为有效的催化剂,以高产率生产新型嘧啶三唑化合物。这些新化合物是由醛、胍、缺电子乙炔类化合物、叔丁基异氰和腙酰氯在水介质中的多组分反应合成的。由于NH基团的存在(使用两种不同的方法进行评估),新合成的嘧啶三唑具有抗氧化性能。此外,使用圆盘分布法对两种不同类型的革兰氏阳性菌和革兰氏阴性菌评估了新产生的嘧啶三唑的抗菌活性,表明使用这些化合物可以防止细菌生长。该方法应用于嘧啶三唑衍生物的制备,反应时间短,产物产率高,并且能够使用简单的程序分离催化剂和产物。
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来源期刊
Molecular Diversity
Molecular Diversity 化学-化学综合
CiteScore
7.30
自引率
7.90%
发文量
219
审稿时长
2.7 months
期刊介绍: Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishes both short and full papers, perspectives, news and reviews dealing with all aspects of the generation of molecular diversity, application of diversity for screening against alternative targets of all types (biological, biophysical, technological), analysis of results obtained and their application in various scientific disciplines/approaches including: combinatorial chemistry and parallel synthesis; small molecule libraries; microwave synthesis; flow synthesis; fluorous synthesis; diversity oriented synthesis (DOS); nanoreactors; click chemistry; multiplex technologies; fragment- and ligand-based design; structure/function/SAR; computational chemistry and molecular design; chemoinformatics; screening techniques and screening interfaces; analytical and purification methods; robotics, automation and miniaturization; targeted libraries; display libraries; peptides and peptoids; proteins; oligonucleotides; carbohydrates; natural diversity; new methods of library formulation and deconvolution; directed evolution, origin of life and recombination; search techniques, landscapes, random chemistry and more;
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