Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375462 | Bioorganic & Medicinal Chemistry Letters | 2005 | 5 Pages |
Several novel 2-imino-5-hydroxymethyl-8-methyl-2H-pyrano[2,3-c]pyridine-3-(N-aryl) carboxamides were prepared by reaction of pyridoxal hydrochloride with various N-arylcyanoacetamides. Reaction of these compounds with aromatic amines furnished a wide series of 2-(N-R-phenyl) imino-5-hydroxymethyl-8-methyl-2H-pyrano[2,3-c]pyridine-3-carboxamides. Antibacterial and antifungal activities of the synthesized compounds were studied. Most of the obtained compounds demonstrated significant activity against bacterial or fungal strains (MIC in the range of 12.5–25 μg/mL), displaying comparable or even better efficacy than the standard drugs.
Graphical abstractSynthesis, antibacterial, and antifungal activities of novel 2H-pyrano[2,3-c]pyridines.Figure optionsDownload full-size imageDownload as PowerPoint slide