Alkylation of 3-methyl-1<Emphasis Type="Italic">H</Emphasis>-acenaphtho[5,6-<Emphasis Type="Italic">de</Emphasis>]pyridazine |
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| Authors: | N I Omelichkin L G Minyaeva V V Mezheritskii |
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| Institution: | 1.Research Institute of Physical and Organic Chemistry at Southern Federal University,Rostov-on-Don,Russia |
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| Abstract: | Alkylation of 3-methyl-1Н-acenaphtho5,6]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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