Strategic Synthesis and Antimycobacterial Evaluation of Coumarin- and Quinoline-Substituted s-Triazine Derivatives via Palladium-Catalyzed Suzuki Coupling
Jyotindra Mahyavanshi, Jayesh M. Pandya, M. R. Solanki
Russian Journal of Organic Chemistry · 2025-03
Abstract
A novel and efficient synthetic pathway was devised for the preparation of 4-{4-anilino-6-[(quinolin-8-yl)oxy]-1,3,5-triazin-2-yl}benzonitriles and 4-{4-anilino-6-[(2-oxo-2H-1-benzopyran-8-yl)oxy]-1,3,5-triazin-2-yl}benzonitriles via palladium-catalyzed Suzuki coupling reaction. This approach allowed precise synthesis of s-triazine derivatives. In vitro antimycobacterial testing against Mycobacterium tuberculosis H37Rv demonstrated notable efficacy, especially of the coumarin derivatives. The structural identity and purity of the products were confirmed through IR, ¹H and ¹³C NMR, and mass spectrometry.
MeSH terms
- Chemistry
- Antimycobacterial
- Quinoline
- Palladium
- Coumarin
- Catalysis
- Combinatorial chemistry
- Triazine
- Coupling (piping)
- Organic chemistry
- Suzuki reaction