Reaction of S-allyl and propargyl derivatives of 2-thiouracils with hydrobromic acid
- Authors: Frolova T.V.1, Kim D.G.1, Sharutin V.V.1, Osheko K.Y.1, Slepukhin P.A.2, Charushin V.N.2
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Affiliations:
- Southern Ural State University
- Institute of Organic Synthesis, Ural Branch
- Issue: Vol 86, No 6 (2016)
- Pages: 1288-1291
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/215245
- DOI: https://doi.org/10.1134/S1070363216060116
- ID: 215245
Cite item
Abstract
Hydrobromic acid reacts with 2-methallylthio- and 2-prenylthio-4(3Н)-pyrimidinones with participation of the double bond to give the products of heterocyclization, and with 2-allylthio- and 2-propargylthio-6-methyl-4(3Н)-pyrimidinones, with the retention of the double bond and the formation of hydrobromides.
About the authors
T. V. Frolova
Southern Ural State University
Author for correspondence.
Email: chemitash@gmail.com
Russian Federation, pr. Lenina 76, Chelyabinsk, 454080
D. G. Kim
Southern Ural State University
Email: chemitash@gmail.com
Russian Federation, pr. Lenina 76, Chelyabinsk, 454080
V. V. Sharutin
Southern Ural State University
Email: chemitash@gmail.com
Russian Federation, pr. Lenina 76, Chelyabinsk, 454080
K. Yu. Osheko
Southern Ural State University
Email: chemitash@gmail.com
Russian Federation, pr. Lenina 76, Chelyabinsk, 454080
P. A. Slepukhin
Institute of Organic Synthesis, Ural Branch
Email: chemitash@gmail.com
Russian Federation, Yekaterinburg
V. N. Charushin
Institute of Organic Synthesis, Ural Branch
Email: chemitash@gmail.com
Russian Federation, Yekaterinburg