One-Pot Synthesis of Some Novel N-Aryl-1,4-Dihydropyridines Derivatives Bearing Nitrogen Mustard

Singala, P.M.; Shah, Viresh H.

doi:10.18052/www.scipress.com/ILCPA.48.61

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One-Pot Synthesis of Some Novel N-Aryl-1,4-Dihydropyridines Derivatives Bearing Nitrogen Mustard

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Abstract:

The synthesis of a novel dihydropyridine, bearing carbethoxy groups at C(3) and C(5), respectively, has been achieved by applying three component Hantzsch-type condensation. The products were assayed for their in vitro biological assay antibacterial activity against with two Gram-positive bacteria Staphylococcus aureus MTCC-96, Streptococcus pyogenes MTCC 443, two Gram-negative bacteria Escherichia coli MTCC 442, Pseudomonas aeruginosa MTCC 441 and three fungal strains Candida albicans MTCC 227, Aspergillus Niger MTCC 282, Aspergillus clavatus MTCC 1323 taking ampicillin, chloramphenicol, ciprofloxacin, norfloxacin, nystatin, and griseofulvin as standard drugs.

Info:

Periodical:

International Letters of Chemistry, Physics and Astronomy (Volume 48)

Pages:

61-67

DOI:

https://doi.org/10.18052/www.scipress.com/ILCPA.48.61

Citation:

P.M. Singala and V. H. Shah, "One-Pot Synthesis of Some Novel N-Aryl-1,4-Dihydropyridines Derivatives Bearing Nitrogen Mustard", International Letters of Chemistry, Physics and Astronomy, Vol. 48, pp. 61-67, 2015

Online since:

March 2015

Authors:

P.M. Singala, Viresh H. Shah

Keywords:

1,4-Dihydropyridine, Antimicrobial Activity, Hantzsch Synthesis

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Creative Commons Attribution 4.0 International License

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Cited By:

[1] D. Malhi, M. Kaur, H. Sohal, "Effect of Substitutions on 1, 4‐Dihdropyridines to Achieve Potential Anti‐Microbial Drugs: A Review", ChemistrySelect, Vol. 4, p. 11321, 2019

DOI: https://doi.org/10.1002/slct.201902354