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3-(5-Phenyl-2H-tetrazol-2-yl)pyridine
3-(5-Phenyl-2H-tetrazol-2-yl)pyridine was synthesized by treating 5-phenyl-1H-tetrazole with pyridin-3-ylboronic acid under Chan–Evans–Lam coupling conditions. The structure and identity were confirmed by 1H, 13C-NMR spectroscopy, IR spectroscopy, UV–Vis spectroscopy, high-resolution mass spectromet...
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| Published in: | MolBank 2023-02, Vol.2023 (1), p.M1598 |
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| container_issue | 1 |
| container_start_page | M1598 |
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| container_volume | 2023 |
| creator | Ershov, Ivan S Esikov, Kirill A Nesterova, Olga M Skryl’nikova, Mariya A Khramchikhin, Andrey V Shmaneva, Nadezda T Chernov, Ivan S Chernova, Ekaterina N Puzyk, Aleksandra M Sivtsov, Eugene V Pavlyukova, Yuliya N Trifonov, Rostislav E Ostrovskii, Vladimir A |
| description | 3-(5-Phenyl-2H-tetrazol-2-yl)pyridine was synthesized by treating 5-phenyl-1H-tetrazole with pyridin-3-ylboronic acid under Chan–Evans–Lam coupling conditions. The structure and identity were confirmed by 1H, 13C-NMR spectroscopy, IR spectroscopy, UV–Vis spectroscopy, high-resolution mass spectrometry, and TLC. The molecular structure was studied experimentally by sequential X-ray diffraction analysis and theoretically by DFT B3LYP quantum chemistry calculation. |
| doi_str_mv | 10.3390/M1598 |
| format | article |
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Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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| subjects | 3-(5-phenyl-2H-tetrazol-2-yl)pyridine Analgesics Analysis Biological activity Chemical synthesis Diffraction Hydrocarbons Identification and classification Infrared spectroscopy Mass spectrometry Methods Molecular structure Nitrogen NMR spectroscopy Nuclear magnetic resonance spectroscopy Pyridine Pyridines Quantum chemistry quantum chemistry calculation Spectrum analysis Structure synthesis Tetrazoles X-ray diffraction analysis X-rays |
| title | 3-(5-Phenyl-2H-tetrazol-2-yl)pyridine |
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