期刊
MOLBANK
卷 2022, 期 3, 页码 -出版社
MDPI
DOI: 10.3390/M1413
关键词
2,6-diaryl-tetrahydroquinolines; trans-methyl-isoeugenol; green Povarov reaction; deep eutectic solvents; N-furoylation; N-(tetrahydroquinolin-1-yl) furancarboxamides
资金
- COLCIENCIAS [110274558597, RC-007-2017]
In this study, a new derivative was synthesized from commercial starting reagents through a two-step procedure. The compound exhibited various important pharmacological properties.
A N-(2,4-diaryltetrahydroquinolin-1-yl) furan-2-carboxamide derivative, [4-(3,4-dimeth-oxyphenyl)-3,6-dimethyl-2-phenyl-3,4-dihydroquinolin-1(2H)-yl)](furan-2-yl)methanone, was synthesized in a two-step procedure from p-toluidine, benzaldehyde, and trans-methyl-isoeugenol as commercial starting reagents through a sequence of Povarov cycloaddition reaction/N-furoylation processes. The structure of the compound was fully characterized by IR, H-1, C-13-NMR, and X-ray diffraction data. Such types of derivatives are known as relevant therapeutic agents exhibiting potent anticancer, antibacterial, antifungal, anti-inflammatory, and immunological modulator properties.
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