Literature DB >> 10321032

Synthesis and antimicrobial activity of substituted imidazolidinediones and thioxoimidazolidinones.

J F Albuquerque1, J A Rocha Filho, S S Brandao, M C Lima, E A Ximenes, S L Galdino, I R Pitta, J Chantegrel, M Perrissin, C Luu-Duc.   

Abstract

Synthesis and physico-chemical properties of new 3-benzyl-4-thioxo-5-arylideneimidazolidine-2-ones and 3-benzyl-5-arylideneimidazolidine-2,4-dione are described. These compounds were synthesized by condensation reaction from aromatic aldehydes and 3-substituted imidazolidine-2,4-diones or 4-thioxoimidazolidine-2-ones. The N-alkylation of 5-benzylideneimidazolidine-2,4-dione led simultaneously to mono- and dialkylated derivatives. The nucleophilic addition of 1-methyl-3-benzylimidazolidine-2,4-dione with 2-cyano-3-(3,4-dichlorophenyl) acrylate also yielded the 3-substituted 5-arylideneimidazolidine-2,4-dione derivative. Antimicrobial in vitro activity was determined on some compounds.

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Year:  1999        PMID: 10321032     DOI: 10.1016/s0014-827x(98)00105-0

Source DB:  PubMed          Journal:  Farmaco        ISSN: 0014-827X


  2 in total

Review 1.  Current advances in the synthesis and biological potencies of tri- and tetra-substituted 1H-imidazoles.

Authors:  Majid M Heravi; Mansoureh Daraie; Vahideh Zadsirjan
Journal:  Mol Divers       Date:  2015-04-12       Impact factor: 2.943

2.  Synthesis and crystal structure of new heterocycles containing 1,2,4-oxadiazole, 1,2,4-oxadiazolone (thione), hydantoin, and mercaptobenzimidazole units.

Authors:  Yaşar Dürüst; Özge Gözlükaya; Gülsün Özer; Frank R Fronczek
Journal:  Mol Divers       Date:  2014-05-04       Impact factor: 2.943

  2 in total

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