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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 5, страницы 630–632 (Mi mendc1275)

Эта публикация цитируется в 2 статьях

Functionalization of 1,2-diphenylpyrazolidine-3,5-dione with polyfluoroalkyl-containing 2- and 3-oxo esters

O. G. Khudina, Ya. V. Burgart, V. I. Saloutin

I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

Аннотация: Fluorine-containing analogues of non-steroidal antiinflammatory drugs Tribuzone and Ketazone have been synthesized by reaction of 1,2-diphenylpyrazolidine-3,5- dione with polyfluoroalkyl-containing 3- and 2-oxo esters. Ethyl 3-(pyrazolidin-4-yl)-3-(polyfluoroalkyl)prop-2-enoates have been obtained as Knoevenagel reaction products from 3-oxo esters in the presence of l-proline. Unlike with 3-oxo esters, addition of ethyl 3,3,3-trifluoro-2-oxopropanoate under basic conditions afforded ethyl 2-(pyrazolidin-4-yl)-3,3,3-trifluoro-2-hydroxypropanoate or its salt without elimination of a water molecule.

Ключевые слова: Knoevenagel reaction, 1,2-diphenylpyrazolidine-3,5-dione, polyfluoroalkyl 3-oxo esters, polyfluoroalkyl 2-oxo esters, non-steroidal anti-inflammatory drugs.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.09.026



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