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Quaternization of 2-Ethoxycarbonylaminopyridine with Phenacylbromides
- Authors: Lomov D.A.1
-
Affiliations:
- Litvinenko Institute of Physical Organic and Coal Chemistry
- Issue: Vol 60, No 8 (2024)
- Pages: 53-56
- Section: Articles
- URL: https://gynecology.orscience.ru/0514-7492/article/view/676687
- DOI: https://doi.org/10.31857/S0514749224080074
- EDN: https://elibrary.ru/RADLZV
- ID: 676687
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Abstract
The interaction of equimolar amounts of 2-ethoxycarbonylaminopyridine with phenacyl bromides in acetonitrile leads to 2-aryl-1-(ethoxycarbonyl)-2-hydroxy-2-phenyl-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromides. When these compounds are boiled in acetic anhydride followed by treatment with potassium carbonate, 2-arylylimidazo[1,2-a]pyridines are formed.
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About the authors
D. A. Lomov
Litvinenko Institute of Physical Organic and Coal Chemistry
Author for correspondence.
Email: lomov_dmitrii@mail.ru
ORCID iD: 0000-0001-9955-6225
Russian Federation, Donetsk
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