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Hydrolysis of Substituted 3-(Thien-2-yl)imino-3H-furan-2-ones and Anti-Inflammatory Activity of the Reaction Products

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Abstract

The hydrolysis of substituted 3-(thien-2-yl)imino-3H-furan-2-ones in the presence of trifluoroacetic acid afforded a series of substituted 4-oxo-2-thienylaminobut-2-enoic acids. Anti-inflammatory activity and acute toxicity of the obtained substituted 4-oxo-2-thienylaminobut-2-enoic acids were studied. It was found that the obtained compounds have a pronounced anti-inflammatory activity and low toxicity.

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Funding

The research was supported by the Perm Research and Education Centre for Rational Use of Subsoil, 2021.

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Correspondence to S. A. Shipilovskikh.

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The studies were performed in accordance with all applicable international, national and institutional guidelines for the care and use of animals. The authors declare no conflicts of interest.

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Translated from Zhurnal Obshchei Khimii, 2021, Vol. 91, No. 10, pp. 1587–1593 https://doi.org/10.31857/S0044460X21100152.

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Shipilovskikh, D.A., Makhmudov, R.R., Rubtsov, A.E. et al. Hydrolysis of Substituted 3-(Thien-2-yl)imino-3H-furan-2-ones and Anti-Inflammatory Activity of the Reaction Products. Russ J Gen Chem 91, 2025–2030 (2021). https://doi.org/10.1134/S1070363221100157

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