Email this article Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine
- Authors: Omelichkin N.I.1, Minyaeva L.G.1, Mezheritskii V.V.1
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Affiliations:
- Research Institute of Physical and Organic Chemistry at Southern Federal University
- Issue: Vol 53, No 2 (2017)
- Pages: 258-262
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215805
- DOI: https://doi.org/10.1134/S1070428017020208
- ID: 215805
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Abstract
Alkylation of 3-methyl-1Н-acenaphtho[5,6]pyridazine with methyl and propyl iodides as well as with benzyl chloride in alkaline medium leads to the formation of the corresponding both N- and С-substituted pyridazine derivatives and also to the dimerization product of the initial compound. The ratio of obtained compounds depends on the used hydride, reaction temperature, and solvent.
About the authors
N. I. Omelichkin
Research Institute of Physical and Organic Chemistry at Southern Federal University
Author for correspondence.
Email: niomelichkin@sfedu.ru
Russian Federation, pr. Stachki 194/2, Rostov-on-Don, 344090
L. G. Minyaeva
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Russian Federation, pr. Stachki 194/2, Rostov-on-Don, 344090
V. V. Mezheritskii
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Russian Federation, pr. Stachki 194/2, Rostov-on-Don, 344090
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