1970Canadian Journal of ChemistryRequires access

Quaternization of quinazoline with methyl iodide

John W. Bunting, William G. Meathrel

Open publisher page 11 citations

Abstract

Contrary to previous reports, the methylation of quinazoline with methyl iodide has been shown to produce both 1-methylquinazolinium iodide and 3-methylquinazolinium iodide. These quaternary salts are formed in the ratio of 5:1 in favor of the latter isomer.

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What this paper is about

Contrary to previous reports, the methylation of quinazoline with methyl iodide has been shown to produce both 1-methylquinazolinium iodide and 3-methylquinazolinium iodide. These quaternary salts are formed in the ratio of 5:1 in favor of the latter isomer.

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OpenAlex reports 11 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Contrary to previous reports, the methylation of quinazoline with methyl iodide has been shown to produce both 1-methylquinazolinium iodide and 3-methylquinazolinium iodide. These quaternary salts are formed in the ratio of 5:1 in favor of the latter isomer.

Key concepts: Chemistry, Methyl iodide, Iodide, Quinazoline, Methylation, Iodine, Medicinal chemistry, Organic chemistry

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