Synthesis of new 4-oxo-1,2,3,4-tetrahydropyrazolo[5,1-с][1,2,4]triazines
- Авторы: Ivanov S.M.1, Mironovich L.M.2, Rodinovskaya L.A.1, Shestopalov A.M.1
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Учреждения:
- N. D. Zelinsky Institute of Organic Chemistry
- Southwestern State University
- Выпуск: Том 67, № 8 (2018)
- Страницы: 1487-1491
- Раздел: Article
- URL: https://journal-vniispk.ru/1066-5285/article/view/242846
- DOI: https://doi.org/10.1007/s11172-018-2244-y
- ID: 242846
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Аннотация
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.
Об авторах
S. Ivanov
N. D. Zelinsky Institute of Organic Chemistry
Автор, ответственный за переписку.
Email: sergey13iv1@mail.ru
Россия, 47 Leninsky prosp., Moscow, 119991
L. Mironovich
Southwestern State University
Email: sergey13iv1@mail.ru
Россия, 94 ul. 50 let Oktyabrya, Kursk, 305040
L. Rodinovskaya
N. D. Zelinsky Institute of Organic Chemistry
Email: sergey13iv1@mail.ru
Россия, 47 Leninsky prosp., Moscow, 119991
A. Shestopalov
N. D. Zelinsky Institute of Organic Chemistry
Email: sergey13iv1@mail.ru
Россия, 47 Leninsky prosp., Moscow, 119991
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