N-arylation of 1,2,4- and 1,3,4-oxadiazolones under the conditions of activitated aromatic nucleophilic substitution
- 作者: Konstantinova A.S1,2, Shetnev A.A1, Volobueva A.S3, Korsakov M.K2
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隶属关系:
- Pharmaceutical Technology Transfer Center, Ushinsky Yaroslavl State Pedagogical University
- Russian State University named after A.N. Kosygin (Technology. Design. Art)
- Saint Petersburg Pasteur Institute
- 期: 卷 59, 编号 11 (2023)
- 页面: 1435-1445
- 栏目: Articles
- URL: https://modernonco.orscience.ru/0514-7492/article/view/667136
- DOI: https://doi.org/10.31857/S0514749223110058
- EDN: https://elibrary.ru/OGQVBA
- ID: 667136
如何引用文章
详细
The possibilities of N -arylation of 1,2,4-oxadiazol-5(4 Н )-ones and 1,3,4-oxadiazol-2(3 Н )-ones with various electron-deficient chloro- and fluorine-substituted nitroarenes under the conditions of classical activated nucleophilic substitution were studied. A significant difference was shown in the reactivity of 1,2,4- and 1,3,4-oxadiazolones in N -arylation reactions. Methods for the synthesis of N-nitroaryl derivatives have been developed.1,2,4- and 1,3,4-oxadiazolones, providing yields of target products with sufficient purity and good yields at the level of 65-96%.
作者简介
A. Konstantinova
Pharmaceutical Technology Transfer Center, Ushinsky Yaroslavl State Pedagogical University;Russian State University named after A.N. Kosygin (Technology. Design. Art)
Email: a.konstantinova@yspu.org
A. Shetnev
Pharmaceutical Technology Transfer Center, Ushinsky Yaroslavl State Pedagogical University
Email: a.shetnev@list.ru
A. Volobueva
Saint Petersburg Pasteur Institute
M. Korsakov
Russian State University named after A.N. Kosygin (Technology. Design. Art)
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