Synthesis and antifungal activity screening of some novel 7–substituted –2–hydroxy–quinoline schiff bases

Journal Title: Journal of Applied Pharmaceutical Research - Year 2016, Vol 4, Issue 4

Abstract

With an objective of synthesizing some novel, potent and broad spectrum antifungal activity having compounds, here some novel quinoline derivatives are reported. Initially 7-substituted-2-cholro-3-formylquinolines were prepared using well known Vilsemeir-Hack reagent method. These on microwave irradiation with 4M HCl yielded 7-substituted-2-hydroxy quinoline-3-carbaldehydes I(a, b), which on further treatment with different substituted hydrazides yielded the novel Schiff bases of quinoline II(a-f). The structure of all newly synthesized compounds was confirmed by spectral study such as IR, 1H NMR, 13C NMR and mass spectroscopy. All the synthesized compounds were screened for in-vitro antifungal activity by two fold serial dilution method using fluconazole as the standard drug. Compounds II a, II b and II d showed significant antioxidant activity.

Authors and Affiliations

M. R. Pradeep Kumar

Keywords

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  • EP ID EP213918
  • DOI -
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How To Cite

M. R. Pradeep Kumar (2016). Synthesis and antifungal activity screening of some novel 7–substituted –2–hydroxy–quinoline schiff bases. Journal of Applied Pharmaceutical Research, 4(4), 5-9. https://europub.co.uk/articles/-A-213918