Reaction of 2-(alkenylsulfanyl)pyrimidin-4(3H)-ones with hydrochloric acid
- Authors: Frolova T.V.1, Kim D.G.1, Slepukhin P.A.2, Osheko K.Y.1
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Affiliations:
- South Ural State University (NRI)
- I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
- Issue: Vol 66, No 4 (2017)
- Pages: 690-693
- Section: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/240433
- DOI: https://doi.org/10.1007/s11172-017-1793-9
- ID: 240433
Cite item
Abstract
Hydrochloric acid reacts with 5-ethyl-2-methallylsulfanyl-6-methylpyrimidin-4(3H)-ones to protonate the nitrogen atom; it adds to the double bond of 2-prenylsulfanyl-6-(trifluoromethyl)pyrimidin-4(3H)-one and gives the addition and heterocyclization products in the case of 2-prenylsulfanyl-6-methylpyrimidin-4(3H)-one.
About the authors
T. V. Frolova
South Ural State University (NRI)
Author for correspondence.
Email: chemitash@gmail.com
Russian Federation, 76 prosp. Lenina, Chelyabinsk, 454080
D. G. Kim
South Ural State University (NRI)
Email: chemitash@gmail.com
Russian Federation, 76 prosp. Lenina, Chelyabinsk, 454080
P. A. Slepukhin
I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences
Email: chemitash@gmail.com
Russian Federation, 22/20 ul. S. Kovalevskoy, Ekaterinburg, 620137
K. Yu. Osheko
South Ural State University (NRI)
Email: chemitash@gmail.com
Russian Federation, 76 prosp. Lenina, Chelyabinsk, 454080