Email this article Synthesis and some transformations of 2-[(4-aminofurazan-3-yl)-1H-1,2,4-triazol-5-yl]acetic acid derivatives
- Authors: Aleksandrova N.S.1, Semyakin S.S.1, Anisimov A.A.2, Struchkova M.I.1, Sheremetev A.B.1
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Affiliations:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Issue: Vol 67, No 11 (2018)
- Pages: 2035-2043
- Section: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/243167
- DOI: https://doi.org/10.1007/s11172-018-2325-y
- ID: 243167
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Abstract
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.
About the authors
N. S. Aleksandrova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
S. S. Semyakin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
A. A. Anisimov
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Russian Federation, 28 ul. Vavilova, Moscow, 119991
M. I. Struchkova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: sab@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
A. B. Sheremetev
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Author for correspondence.
Email: sab@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
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