Sulaiman E, Al-Masri E, Alhawarri MB, Ibrahim MM, Al-Refai M, Ali BF, Shuaib A (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 23
Article Number: e71718
Journal Issue: 9
DOI: 10.1002/cbdv.71718
This study presents the formation of 2-methoxy-3-cyanopyridine derivatives 3(a–g) that occurred while attempting to synthesize furo[2,3-b]pyridines. The structures of all newly synthesized compounds were confirmed by IR, 1H NMR, 13C NMR, 2D-NMR, HRMS, and crystal x-ray structure analysis. In the crystal structure of 3f, the molecules are connected by C―H···N≡C, C―Cl···O―C, and C―S···N≡C interactions to form layers, which are further connected through π···π and Cl···π interactions, consolidating a 3-dimensional structure. The antioxidant activities of all synthesized compounds were tested in a DPPH (2,2-diphenyl-1-picrylhydrazyl) free radical scavenger assay. Compound 3d displayed the highest level of activity with an IC
APA:
Sulaiman, E., Al-Masri, E., Alhawarri, M.B., Ibrahim, M.M., Al-Refai, M., Ali, B.F., & Shuaib, A. (2026). Synthesis, Characterization, and Biological Assessment of 2-Methoxynicotinonitrile Derivatives. Chemistry & Biodiversity, 23(9). https://doi.org/10.1002/cbdv.71718
MLA:
Sulaiman, Eman, et al. "Synthesis, Characterization, and Biological Assessment of 2-Methoxynicotinonitrile Derivatives." Chemistry & Biodiversity 23.9 (2026).
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