CHACONE APPLICATION IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF ISOXAZOLO, THIONE, AND PYRIMIDO SUBSTITUTED ANALOGIES OF 2-BENZYLIDENE CYCLOPENTANONE

  • Unique Paper ID: 209140
  • Volume: 13
  • Issue: 5
  • PageNo: 864-867
  • Abstract:
  • New series of isoxazole and benzodizepine compounds were synthesised from chalcones and their antibacterial activity was evaluated. First, chalcones were created by reacting Utilising Claisen-Schimidt condensation, Benz aldehyde is combined with various acetophenones. In ethanol, chalcone was utilised to react with sodium acetate, hydroxylamine hydrochloride, and other isoxazole derivatives. In addition, piperidine was utilised to react with o-phenylenediamine in ethanol to produce derivatives of benzodizepine. The structures of the freshly synthesised isoxazole and benzodiazepine derivatives have been developed based on their spectrum data. The synthesised versions of the selected compounds' antibacterial efficacy were evaluated. Cyclopentanone was combined with a number of aromatic aldehydes to form chalcones. When urea, thiurea, and hydroxylamine hydrochloride are used to treat these chalcones.

Copyright & License

Copyright © 2026 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

BibTeX

@article{209140,
        author = {Prof.Tushar.V.Pawar},
        title = {CHACONE APPLICATION IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF ISOXAZOLO, THIONE, AND PYRIMIDO SUBSTITUTED ANALOGIES OF 2-BENZYLIDENE CYCLOPENTANONE},
        journal = {International Journal of Innovative Research in Technology},
        year = {2026},
        volume = {13},
        number = {5},
        pages = {864-867},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=209140},
        abstract = {New series of isoxazole and benzodizepine compounds were synthesised from chalcones and their antibacterial activity was evaluated. First, chalcones were created by reacting Utilising Claisen-Schimidt condensation, Benz aldehyde is combined with various acetophenones. In ethanol, chalcone was utilised to react with sodium acetate, hydroxylamine hydrochloride, and other isoxazole derivatives. In addition, piperidine was utilised to react with o-phenylenediamine in ethanol to produce derivatives of benzodizepine. The structures of the freshly synthesised isoxazole and benzodiazepine derivatives have been developed based on their spectrum data. The synthesised versions of the selected compounds' antibacterial efficacy were evaluated. Cyclopentanone was combined with a number of aromatic aldehydes to form chalcones. When urea, thiurea, and hydroxylamine hydrochloride are used to treat these chalcones.},
        keywords = {chalcones, isoxazoles, pyrimido, thione, antimicrobial activity.},
        month = {October},
        }

Cite This Article

Prof.Tushar.V.Pawar, (2026). CHACONE APPLICATION IN HETEROCYCLIC SYNTHESIS: SYNTHESIS OF ISOXAZOLO, THIONE, AND PYRIMIDO SUBSTITUTED ANALOGIES OF 2-BENZYLIDENE CYCLOPENTANONE. International Journal of Innovative Research in Technology (IJIRT), 13(5), 864–867.

Related Articles