Literature DB >> 1368273

Synthesis and application of novel sulpha drugs based on quinoxaline-2-one and/or quinoxaline-2-thione.

I M Awad1.   

Abstract

Some novel azo-Sulpha drugs as 3-methyl-N-azo-(4'-substituted heterocyclo-benzene-sulphamoyl) quinoxaline-2-ones (1-11) and 3-methyl-N-azo-(4'-substituted heterocyclo-benzene-sulphamoyl)-quinoxaline-2-thiones (1'-11') were synthesized by coupling 4'-substituted heterocyclo-benzene-sulphamoyl diazonium acetates with 3-methyl-N-(1H)-quinoxaline-2-one and/or with 3-methyl-N(1H) quinoxaline-2-thione in acid medium. The corresponding iron (III) (1a-11, 1'a-11'a) copper (II) (1b-1b'-7b') and mercury (II) (1c-11c, 1c'-11c) chelates were also prepared in a 1:1 metal-to-ligand ratio. The ligands and their chelates were characterized on the basis of microanalysis, UV, IR and H'-NMR spectrometry, and were tested in vitro for their antibacterial and antifungal activities.

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Year:  1992        PMID: 1368273     DOI: 10.1002/jctb.280530303

Source DB:  PubMed          Journal:  J Chem Technol Biotechnol        ISSN: 0268-2575            Impact factor:   3.174


  1 in total

1.  One-pot synthesis of biologically active 1,2,3-trisubstituted pyrrolo[2,3-b]quinoxalines through a palladium-catalyzed reaction with internal alkyne moieties.

Authors:  Ali Keivanloo; Tayebeh Besharati-Seidani; Babak Kaboudin; Akihiro Yoshida; Tsutomu Yokomatsu
Journal:  Mol Divers       Date:  2018-06-16       Impact factor: 2.943

  1 in total

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