Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine
- Авторы: Omelichkin N.I.1, Minyaeva L.G.1, Mezheritskii V.V.1
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Учреждения:
- Research Institute of Physical and Organic Chemistry at Southern Federal University
- Выпуск: Том 53, № 2 (2017)
- Страницы: 258-262
- Раздел: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215805
- DOI: https://doi.org/10.1134/S1070428017020208
- ID: 215805
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Аннотация
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.
Об авторах
N. Omelichkin
Research Institute of Physical and Organic Chemistry at Southern Federal University
Автор, ответственный за переписку.
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
L. Minyaeva
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
V. Mezheritskii
Research Institute of Physical and Organic Chemistry at Southern Federal University
Email: niomelichkin@sfedu.ru
Россия, pr. Stachki 194/2, Rostov-on-Don, 344090
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