Alkylation of 3-methyl-1H-acenaphtho[5,6-de]pyridazine


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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.

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N. Omelichkin

Research Institute of Physical and Organic Chemistry at Southern Federal University

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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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