The present paper describes the simple and efficient protocol for the synthesis of 2-Chloro/Marcapto-quinolin fused-1,6-Dihydropyridine Derivatives (2a-d/3a-d) by (Et3N) and (NaOEt) catalyzed three-component one pot reaction of amine, aldehyde and ketones. The newly synthesized compounds were systematically characterized by Fourier-Transform Infrared Spectroscopy (FT-IR), Proton Nuclear Magnetic Resonance (1H-NMR), elemental analysis, and mass spectral analysis. The antibacterial potency of these compounds was tested against Gram-positive and Gram-negative bacteria. The sulfur containing quinoline compound 3a showed significant inhibitory effect on Staphylococcus aureus, Escherichia coli and Streptococcus pyogenes in consistent to halogen containing quinoline compound 2a.
Select your language of interest to view the total content in your interested language
Der Pharma Chemica received 15261 citations as per Google Scholar report