RUS  ENG
Полная версия
ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2023, том 33, выпуск 2, страницы 194–196 (Mi mendc347)

Эта публикация цитируется в 3 статьях

Communications

Synthesis of new analgesics based on 4-isopropyl-1-phenyl-3-(trifluoromethyl)pyrazol-5-one

L. S. Lapshina, E. V. Shchegolkova, Ya. V. Burgarta, G. A. Triandafilovab, O. P. Krasnykhb, K. O. Malyshevab, V. I. Saloutina

a I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Perm National Research Polytechnic University, Perm, Russian Federation


Аннотация: Methyl 4-trifluoro-2-isopropyl-4-oxobutanoate prepared by the improved procedure was cyclized with hydrazines to afford the title pyrazole derivatives. N- and O-alkylation of 4-isopropyl-1-phenyl-3-(trifluoromethyl)pyrazol-5-ol gave trifluoromethyl analogues of Propyphenazone and 5-alkoxy derivatives. 4-Isopropylpyrazoles containing O-butoxy moiety with a terminal trifluoromethyl or acyloxy group were found to demonstrate a promising analgesic activity.

Ключевые слова: 4-isopropyl-3-(trifluoromethyl)pyrazol-5-ols, alkylation, propyphenazone, 5-alkoxypyrazoles, organofluorine compounds, analgesic activity, acute toxicity.

Язык публикации: английский

DOI: 10.1016/j.mencom.2023.02.014



© МИАН, 2025