Author:
Moirangthem Nimalini Devi,Laitonjam Warjeet Singh
Abstract
A new and facile synthesis of 2-thioxoquinazolin-4-ones by introducing a benzenoid system in the pyrimidine moiety by reacting ethoxymethylene derivatives of 1,3-diarylthiobarbituric acids (DTBA) with active methylene compounds, such as malononitrile and ethyl cyanoacetate, in presence of ZnCl2 has been developed.
Cited by
8 articles.
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1. Construction of Biologically Active Five- and Six-Membered Fused Ring Pyrimidine Derivatives from 1,3-Diarylthiobarbituric Acids (DTBA);Strategies Towards the Synthesis of Heterocycles and Their Applications [Working Title];2022-12-09
2. Surfactant based nanoreactor micellar assembly: An innovative route for synthesis of 2-thioxo-2,3-dihydroquinazolin-4(1H)-ones;Journal of Molecular Liquids;2022-08
3. An expedient metal-free cascade route to chromonyl diene scaffolds: thermodynamic vs. kinetic control;RSC Advances;2022
4. Synthesis, Antimicrobial and Antioxidant Activities of Novel 7-thioxo- 4,6,7,8-tetrahydro-pyrazolo[4',3':5,6]pyrano[2,3-d]pyrimidin-5(1H)-ones Derived by SDS Catalyzed Multicomponent Reactions in Aqueous Micellar Media;The Natural Products Journal;2018-09-17
5. Trisubstituted barbiturates and thiobarbiturates: Synthesis and biological evaluation as xanthine oxidase inhibitors, antioxidants, antibacterial and anti-proliferative agents;European Journal of Medicinal Chemistry;2018-01