Preparation and synthetic scope of 3-(4-methyl-2-R-pyrimidin-5-yl)-3-oxopropionic esters View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-09

AUTHORS

A. Yu. Potapov, A. V. Falaleev, Kh. S. Shikhaliev, G. V. Shatalov

ABSTRACT

A condensation of 2-R-5-acetyl-4-methylpyrimidines with dimethyl carbonate led to a number of 3-(2-R-4-methylpyrimidin-5-yl)-3-oxopropionic esters, which reacted with (piperidin-1-yl)carboxamidine and arylguanidines to give 2-R′-6-(2-R-4-methylpyrimidin-5-yl)-3H-pyrimidin-4-ones. A reaction of 3-(2-R-4-methylpyrimidin-5-yl)-3-oxopropionic esters with hydrazines led to the formation of 3-(2-R-4-methylpyrimidin-5-yl)-2-R″-1,2-dihydropyrazol-3-ones.

PAGES

2198-2200

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-014-0720-6

DOI

http://dx.doi.org/10.1007/s11172-014-0720-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1051105069


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