3-(5-Phenyl-2H-tetrazol-2-yl)pyridine-Reference-Cited by-同舟云学术

3-(5-Phenyl-2H-tetrazol-2-yl)pyridine

Published:2023-02-28 Issue:1 Volume:2023 Page:M1598
ISSN:1422-8599
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language:en
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Author:

Ershov Ivan S.¹,Esikov Kirill A.¹,Nesterova Olga M.¹,Skryl’nikova Mariya A.¹²,Khramchikhin Andrey V.²^ORCID,Shmaneva Nadezda T.¹,Chernov Ivan S.¹,Chernova Ekaterina N.³^ORCID,Puzyk Aleksandra M.⁴^ORCID,Sivtsov Eugene V.⁵^ORCID,Pavlyukova Yuliya N.¹,Trifonov Rostislav E.¹,Ostrovskii Vladimir A.¹³^ORCID

Affiliation:

1. Department of Chemistry and Technology of Nitrogen-Containing Organic Compounds, Saint Petersburg State Institute of Technology (Technical University), 24-26/49 Moskovsky Ave., 190013 St. Petersburg, Russia

2. Department of Organic Chemistry, Saint Petersburg State Institute of Technology (Technical University), 24-26/49 Moskovsky Ave., 190013 St. Petersburg, Russia

3. Saint Petersburg Federal Research Center of the Russian Academy of Sciences (SPC RAS), 39, 14th Line, 199178 St. Petersburg, Russia

4. Research Park, Saint Petersburg State University, 26 Universitetskii Prospect, Petergof, 198504 St. Petersburg, Russia

5. Department of Physical Chemistry, Saint Petersburg State Institute of Technology (Technical University), 24-26/49 Moskovsky Ave., 190013 St. Petersburg, Russia

Abstract

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.

Funder

Russian Foundation for Basic Research

grant program for young scientists FASIE

Publisher

MDPI AG

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://www.mdpi.com/1422-8599/2023/1/M1598/pdf

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