Chemical properties of 3-tert-butyl-2-oxo1,2-dihydropyrrolo[1,2-b][1,2,4]triazin-6-carboxylates
- Авторлар: Ivanov S.M1, Koltun D.S1, Kolotyrkina N.G1
-
Мекемелер:
- N.D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences
- Шығарылым: Том 59, № 4 (2023)
- Беттер: 492-506
- Бөлім: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/666314
- DOI: https://doi.org/10.31857/S0514749223040080
- EDN: https://elibrary.ru/ASIKVD
- ID: 666314
Дәйексөз келтіру
Аннотация
Alkaline hydrolysis of 6- tert -butyl-8-ethyl-7-amino-3- tert -butyl-2-oxo-1,2-dihydropyrrolo[1,2- b ][1,2,4]triazin6,8-dicarboxylate gave the corresponding 8-carboxylic acid, treatment of which with n -BuBr or NBS/TEA led to the decarboxylation and alkylation of N1, C2O or bromination of the C8 ring position, respectively. Diazotization of 7-amino-3- tert -butyl-8-R1-2-ОR2-pyrrolo[1,2- b ][1,2,4]triazin-6-carboxylates furnished 7-azido (R1 = Br, CO2Et;R1 = H, n -Bu) and 7-unsubstituted (R1 = Br, CN; R2 = n -Bu, CH2CO2Et, CH2Boc) derivatives, and also 7-(1 H -1,2,3-triazol-1-yl)pyrrolo[1,2- b ][1,2,4]triazin-6,8-dicarboxylate. The spectral and X-Ray structural features, as well as antimicrobial activity of the synthesized compounds are considered.
Негізгі сөздер
Авторлар туралы
S. Ivanov
N.D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences
Email: sergey13iv1@mail.ru
D. Koltun
N.D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences
Email: sergey13iv1@mail.ru
N. Kolotyrkina
N.D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences
Email: sergey13iv1@mail.ru
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