Synthesis and Some Transformations of 7-Substituted 8-Chlorotheophyllines
- Authors: Petrova K.Y.1, Kim D.G.1, Sharutin V.V.1, Eltsov O.S.2, Shtukina T.S.2, Anuchin A.A.3
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Affiliations:
- South Ural State University (NRU)
- Ural Federal University
- Criminalistics Laboratory of Police Department of Chelyabinsk Region
- Issue: Vol 89, No 11 (2019)
- Pages: 2201-2206
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223151
- DOI: https://doi.org/10.1134/S1070363219110069
- ID: 223151
Cite item
Abstract
Alkylation of 8-chlorotheophylline by alkenyl(propargyl) halides yields 7-alkenyl(propargyl)-8-chlorotheophyllines. The reaction of 8-chlorotheophylline with 1,3-dichloropropan-2-ol leads to the formation of oxazolo[2,3-f]purinium system. 7-Alkenyl-8-chlorotheophyllines react with bromine to give dibromoalkyl-8-chlorotheophyllines. The reaction of 7-methallyl-8-chlorotheophylline with m-chloroperbenzoic acid affords the corresponding oxirane.
About the authors
K. Yu. Petrova
South Ural State University (NRU)
Author for correspondence.
Email: osheko_kseniya@mail.ru
Russian Federation, Chelyabinsk, 454080
D. G. Kim
South Ural State University (NRU)
Email: osheko_kseniya@mail.ru
Russian Federation, Chelyabinsk, 454080
V. V. Sharutin
South Ural State University (NRU)
Email: osheko_kseniya@mail.ru
Russian Federation, Chelyabinsk, 454080
O. S. Eltsov
Ural Federal University
Email: osheko_kseniya@mail.ru
Russian Federation, Yekaterinburg, 620075
T. S. Shtukina
Ural Federal University
Email: osheko_kseniya@mail.ru
Russian Federation, Yekaterinburg, 620075
A. A. Anuchin
Criminalistics Laboratory of Police Department of Chelyabinsk Region
Email: osheko_kseniya@mail.ru
Russian Federation, Chelyabinsk, 454091