Synthesis and some transformations of 2-[(4-aminofurazan-3-yl)-1H-1,2,4-triazol-5-yl]acetic acid derivatives
- Авторы: Aleksandrova N.S.1, Semyakin S.S.1, Anisimov A.A.2, Struchkova M.I.1, Sheremetev A.B.1
-
Учреждения:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Выпуск: Том 67, № 11 (2018)
- Страницы: 2035-2043
- Раздел: Full Articles
- URL: https://journal-vniispk.ru/1066-5285/article/view/243167
- DOI: https://doi.org/10.1007/s11172-018-2325-y
- ID: 243167
Цитировать
Аннотация
Two methods for the synthesis of 1,2,4-triazolylacetic ester bearing an aminofurazanyl substituent at the position 5 were developed. The triazole cycle was formed via the cyclocondensation of 3-aminofurazanecarboxylic acid hydrazide or amidrazone with ethoxycarbonylethyl acetimidate hydrochloride.
Об авторах
N. Aleksandrova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
S. Semyakin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
A. Anisimov
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Россия, 28 ul. Vavilova, Moscow, 119991
M. Struchkova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
A. Sheremetev
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Автор, ответственный за переписку.
Email: sab@ioc.ac.ru
Россия, 47 Leninsky prosp., Moscow, 119991
Дополнительные файлы
