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Stream/Area:
-
Subject:
-
Paper ID:
IJSREM63778
Volume:
10 |
5 |
May 2026
Pages:
1-9
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
Department of Chemistry
PRISM PG & DG College
Department of Chemistry
PRISM PG & DG College
Department of Chemistry
PRISM PG & DG College
Department of Chemistry
PRISM PG & DG College
This study synthesized a novel series of 5-phenyl-5,7,8,9-tetrahydro-6H-[1,3,4] thiadiazolo [2,3-b]quinazolin-6-one using Cu(OAc)2 a novel catalyst. A one-pot multicomponent synthesis reaction involving dimedone, substituted aromatic aldehydes, and 5-(4-nitrophenyl)-1, 3, 4-thiadiazol-2-amine in the presence of ethanol as a solvent, which generated a variety of new thiadiazolo [2,3-b]quinazolin-6-one scaffolds. This component can be made by refluxing semithiocarbazide with 4-nitrobenzoic acid in the presence of ethanol and sulfuric acid. A low E-factor, high reaction mass efficiency, atom economy, scalability, and rapid reaction time are just a few of the notable benefits of this freshly discovered technology. In addition to invitro study of antimicrobial activity evaluated of titled derivatives..
KEYWORDS
To generate a series of thiadiazolo[2,3-b] quinazolin-6-ones, a one-pot, one-step, multicomponent reaction involving dimedone, substituted aromatic aldehydes, and 5-aryl-1,3,4-thiadiazol-2-amines in the presence of Cu(OAc)2 under solvent conditions like ethanol has been devised. This procedure is quick, simple, practical, and eco-friendly. High to exceptional yields, high reaction speeds, avoidance of hazardous organic solvents, simplicity of use, simple catalyst recycling and separation, appropriateness for large-scale synthetic applications, generation of water as green waste, and superior atom economy and the evaluation of antimicrobial activity
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Publication Date
5/22/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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