Abstract

The compounds bearing naphthalene moiety can be used as medical preparations because of their wide spectrum of biological activity and low toxicity. In this study, a new series of azoles or azines were synthesized from the reaction of the key intermediate 1-(1-hydroxynaphthalen-2-yl)-3-phenylpropane-1,3-dione 3 with a variety of electrophilic and nucleophilic reagents under a variety of mild conditions. The chemical structures of these compounds were confirmed by various spectroscopic methods such as (IR, 1H-NMR, 13C-NMR, mass spectra and elemental analyses). The prepared compounds were screened in vitro for their anti-microbial activity against some species of Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and Gram-negative bacteria (Escherichia coli and Pseudomonas aeuroginosa). Anti-fungal activities of the compounds were tested against yeast and mycelial fungi,Candida albicans and Aspergillus flavus. The antimicrobial activity of this series was showed either weak or moderate activities.Graphic abstract

Highlights

  • According to the literature survey, heterocyclic compounds containing nitrogen, sulfur and oxygen atom are found to possess a varity of biological activities

  • Various biological applications have been reported for pyrazoles such as anti-viral [1], anti-cancer [2], anti-microbial [3], anti-inflammatory [4], anti-depressant [5] anti-convulsant [6] analgesic and antiplatelet [7, 8]

  • Cyanopyridine derivatives have attracted considerable attention as they appeared of interest to possess anti-cancer [9], anti-convulsant [10] and anti-microbial [11]

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Summary

Introduction

According to the literature survey, heterocyclic compounds containing nitrogen, sulfur and oxygen atom are found to possess a varity of biological activities. The mass spectrum of compound 3 is in agreement with the proposed structure, its showed a molecular ion peak at m/z = 290 ­(M+) corresponding to a molecular formula ­C19H14O3 (Scheme 1).

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