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Synthesis of novel 2,4,6-trisubstituted pyrimidine derivatives and their in vitro antimicrobial activity

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Abstract

A series of novel pyrimidines (6a–6i) has been synthesized from corresponding chalcones and isonicotinimidamide.HCl in the presence of potassium carbonate involving Michael addition followed by cycloaddition. All newly synthesised chalcones and pyrimidines were screened for in vitro antimicrobial activity against various Gram positive, Gram negative bacterial and fungal strains. Most of compounds displayed high antimicrobial activity compared to standard drugs Penicillin, Streptomycin and Ampothericin-B.

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Authors and Affiliations

  1. Department of Chemistry, Osmania University, Hyderabad, 500007, India

    D. Ashok & D. Mohan Gandhi

  2. Richmond Vivek Laboratories, Mallapur, Hyderabad, 500076, India

    R. Suneel Kumar

  3. Centre for Chemical Science and Technology, IST, JNTUH, Hyderabad, 500085, India

    A. Jayashree

Authors
  1. D. Ashok
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  2. R. Suneel Kumar
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  3. D. Mohan Gandhi
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  4. A. Jayashree
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Correspondence to D. Ashok.

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The text was submitted by the authors in English.

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Ashok, D., Kumar, R.S., Mohan Gandhi, D. et al. Synthesis of novel 2,4,6-trisubstituted pyrimidine derivatives and their in vitro antimicrobial activity. Russ J Gen Chem 86, 1396–1404 (2016). https://doi.org/10.1134/S1070363216060268

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  • DOI: https://doi.org/10.1134/S1070363216060268

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