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

被引:5
作者
Hezarcheshmeh, Nasrin Karami [1 ]
Godarzbod, Farideh [1 ]
Abdullah, Media Noori [2 ]
Hossaini, Zinatossadat [3 ]
机构
[1] Islamic Azad Univ, Dept Chem, Sci & Res Branch, Tehran, Iran
[2] Salahaddin Univ Erbil, Coll Sci, Dept Chem, Erbil, Kurdistan Regio, Iraq
[3] Islamic Azad Univ, Dept Chem, Qaemshahr Branch, Qaemshahr, Iran
关键词
Pyrimidine triazoles; Multicomponent reaction; Alkyl bromide; Activated acetylenic compounds; IN-VITRO ANTITUMOR; DIASTEREOSELECTIVE SYNTHESIS; ANTIMICROBIAL ACTIVITY; ACTIVATED ACETYLENES; EFFICIENT CATALYST; PHOSPHONATE ESTERS; ORGANIC-SYNTHESIS; AQUEOUS-SOLUTION; DRUG-DELIVERY; GLUTAMIC-ACID;
D O I
10.1007/s11030-023-10754-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:217 / 228
页数:12
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