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2000
Volume 3, Issue 3
  • ISSN: 2213-3356
  • E-ISSN: 2213-3364

Abstract

Background: The Present work describe the synthetic protocol of a new series of 2-(4-(2-(5- Ethylpyridin-2-yl)ethoxy)phenyl)-4-(4-substituted)-2,3-dihydrobenzo [b][1,4]thiazepine (5a-j) by the cyclization of chalcones (4a-j) with 2-amino thiophenol by microwave induced solvent free conditions as well as conventional approach. Methods: The elemental analysis and spectral method (IR, 1H and 13C NMR) were characterized the structure of all synthesized compounds. Result: These compounds were screened for antibacterial and antifungal activity. Bezothiazepine derivative 5f showed potency (MBC = 50 μg/ml) against gram negative P. aeruginosa and 5i displyed encouraging activity (MFC = 200 μg/ml) against A. niger and A. clavatus. Conclusion: The solvent less non-conventional microwave induced synthesis of compound (5a-j) has been proven considerable advantageous over conventional methods.

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/content/journals/cmic/10.2174/2213335603666160609123550
2016-09-01
2025-10-14
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  • Article Type:
    Research Article
Keyword(s): Antibacterial; antifungal; benzothiazepine; chalcone; microwave; solvent-free
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