Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine
- 作者: Omelichkin N.I.1, Minyaeva L.G.1, Mezheritskii V.V.1
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隶属关系:
- Research Institute of Physical and Organic Chemistry at Southern Federal University
- 期: 卷 53, 编号 2 (2017)
- 页面: 258-262
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215805
- DOI: https://doi.org/10.1134/S1070428017020208
- ID: 215805
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详细
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.
作者简介
N. Omelichkin
Research Institute of Physical and Organic Chemistry at Southern Federal University
编辑信件的主要联系方式.
Email: niomelichkin@sfedu.ru
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090
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