Reactions of 2-AMINO-6-METHYLPYRIMIDINONES-4 with ALKYL HALIDES C4-C9

dc.contributor.author	Kh. I. Nurbayev
dc.contributor.author	N. À. Kuchkarov
dc.date.accessioned	2025-12-30T07:50:36Z
dc.date.issued	2024-02-24
dc.description.abstract	Alkylation of 2-amino-6-methylpyrimidine-4-one alkyl halides C4-C9 was performed. It is shown that, depending on the reaction conditions and the ratio of reagents, N3-alkylation products occur. It was found that, unlike methyl iodide, methyltosylate, alkylation of 2-amino-6-methylpirimidine-4-one alkyl halides C4-C9 in absolute alkoholproceeds with the formation of a mixture of isomeric N3-O4 alkyl products.
dc.format	application/pdf
dc.identifier.uri	https://europeanscience.org/index.php/3/article/view/447
dc.identifier.uri	https://asianeducationindex.com/handle/123456789/27403
dc.language.iso	eng
dc.publisher	European Science Publishing
dc.relation	https://europeanscience.org/index.php/3/article/view/447/440
dc.rights	https://creativecommons.org/licenses/by-nc/4.0
dc.source	European Science Methodical Journal; Vol. 2 No. 2 (2024): ESMJ; 75-78
dc.source	2938-3641
dc.subject	2-amino-6-methylpirimidin-4-one, C4-C9.
dc.title	Reactions of 2-AMINO-6-METHYLPYRIMIDINONES-4 with ALKYL HALIDES C4-C9
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.type	Peer-reviewed Article

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