Synthesis of new 4-oxo-1,2,3,4-tetrahydropyrazolo[5,1-с][1,2,4]triazines
- Authors: Ivanov S.M.1, Mironovich L.M.2, Rodinovskaya L.A.1, Shestopalov A.M.1
-
Affiliations:
- N. D. Zelinsky Institute of Organic Chemistry
- Southwestern State University
- Issue: Vol 67, No 8 (2018)
- Pages: 1487-1491
- Section: Article
- URL: https://journal-vniispk.ru/1066-5285/article/view/242846
- DOI: https://doi.org/10.1007/s11172-018-2244-y
- ID: 242846
Cite item
Abstract
Alkylation of 7-amino-3-tert-butyl-4-oxo-4,6-dihydropyrazolo[5,1-c][1,2,4]triazine-8-carbonitrile led to N1-substituted derivative, which upon treatment with NaH and MeI in DMF was converted to 1-benzyl-3-tert-butyl-7-dimethylamino-4-oxo-1,4-dihydropyrazolo-[5,1-c][1,2,4]triazine-8-carbonitrile. The latter reacted with Grignard reagents to give high yields of new 3-tert-butyl-3-R-4-oxo-1,2,3,4-tetrahydropyrazolo[5,1-c][1,2,4]triazines (R = Alk, Ph). The reaction course and conditions were studied, and spectral characteristics of the products are discussed.
About the authors
S. M. Ivanov
N. D. Zelinsky Institute of Organic Chemistry
Author for correspondence.
Email: sergey13iv1@mail.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
L. M. Mironovich
Southwestern State University
Email: sergey13iv1@mail.ru
Russian Federation, 94 ul. 50 let Oktyabrya, Kursk, 305040
L. A. Rodinovskaya
N. D. Zelinsky Institute of Organic Chemistry
Email: sergey13iv1@mail.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
A. M. Shestopalov
N. D. Zelinsky Institute of Organic Chemistry
Email: sergey13iv1@mail.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
Supplementary files
