Evaluation of Quinazolin-2,4-Dione Derivatives as Promising Antibacterial Agents: Synthesis, In Vitro, In Silico ADMET and Molecular Docking Approaches.

ABSTRACT: A series of new quinazolin-2,4-dione derivatives incorporating amide/eight-membered nitrogen-heterocycles 2a-c, in addition, acylthiourea/amide/dithiolan-4-one and/or phenylthiazolidin-4-one 3a-d and 4a-d. The starting compound 1 was prepared by reaction of 4-(2,4-dioxo-1,4-dihydro-2H-quinazolin-3-yl)-benzoyl chloride with ammonium thiocyanate and cyanoacetic acid hydrazide. The reaction of 1 with strong electrophiles, namely, o-aminophenol, o-amino thiophenol, and/or o-phenylene diamine, resulted in corresponding quinazolin-2,4-dione derivatives incorporating eight-membered nitrogen-heterocycles 2a-d. Compounds 3a-d and 4a-d were synthesized in good-to-excellent yi

SUBMITTER: Abdelmonsef AH 

PROVIDER: S-EPMC11643521 | biostudies-literature | 2024 Nov

REPOSITORIES: biostudies-literature