4.5 Article

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

Journal

MOLECULAR DIVERSITY
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11030-023-10754-z

Keywords

Pyrimidine triazoles; Multicomponent reaction; Alkyl bromide; Activated acetylenic compounds

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This research aims to synthesize novel pyrimidine triazole compounds efficiently using triethylamin as a catalyst. The newly synthesized compounds exhibit antioxidant and antibacterial properties, making them potentially valuable in various applications.
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.

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