SFHS: Reusable catalyst for the synthesis of polyhydroquinoline derivatives and its molecular docking studies against tyrosine protein kinase

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  • Amit Waghmare1,
  • Tushar Patil2,
  • Kailash Kadam3,
  • Shivaji Sandu Pandit3,
  1. Post Graduate and Research Centre, Department of Chemistry, Padmashri Vikhe Patil College of Arts, Science and Commerce, Pravaranagar, Dist. Ahmednagar-413713 (MS), India
  2. Department of Biotechnology,PVP College, Pravaranagar, Tal.Rahata-413 713
  3. Department of Chemistry, PVP College, Pravaranagar, Tal.Rahata-413 713

Published in Issue 2024-02-03

How to Cite

Waghmare, A., Patil, T., Kadam, K., & Pandit, S. S. (2024). SFHS: Reusable catalyst for the synthesis of polyhydroquinoline derivatives and its molecular docking studies against tyrosine protein kinase. Iranian Journal of Catalysis, 5(1). https://oiccpress.com/ijc/article/view/3825

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Abstract

An efficient synthesis of polyhydroquinoline derivatives is achieved via Hantzsch condensation reaction between aldehydes, dimedone, ethyl acetoacetate and ammonium acetate in the presence of catalytic amount of SFHS in ethanol. This method gives remarkable advantages such as shorter reaction time, simple workup procedure and good to excellent yields. Furthermore the catalyst can be recovered conveniently and reused efficiently. To analyze potential anticancer activity, synthesized derivatives were docked to tyrosine protein kinase (1YJ) against 4ST and PTR binding sites.

Keywords

  • Molecular docking,
  • Multicomponent reaction,
  • Polyhydroquinoline derivatives,
  • Silica supported ferric hydrogen sulphate
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