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Synthesis and Antioxidant Activity of N -Aminomethyl Derivatives of Ethosuximide and Pufemide Anticonvulsants
Russian Journal of General Chemistry ( IF 0.9 ) Pub Date : 2020-06-04 , DOI: 10.1134/s1070363220030093
N. Z. Hakobyan , Z. A. Hovasyan , S. S. Hovakimyan , A. G. Melkonyan , N. A. Pagutyan , G. A. Panosyan , G. A. Gevorgyan

Abstract

Aminomethylation of 3-methyl-3-ethylpyrrolidin-2,5-dione (ethosuximide) and 3-(4-isopropoxyphenyl)pyrrolidine-2,5-dione (pufemide) with a 25% aqueous formalin solution and alkyl(aryl)amines yielded corresponding N-aminomethyl derivatives. The antioxidant activity of the synthesized compounds and their effect on some parameters of the blood coagulation system were studied.


中文翻译:

乙草胺和布非胺抗惊厥药的N-氨基甲基衍生物的合成及抗氧化活性

摘要

用25%的福尔马林水溶液和烷基(芳基)胺将3-甲基-3-乙基吡咯烷酮2,5-二酮(ethosuximide)和3-(4-异丙氧基苯基)吡咯烷-2,5-dione(pufemide)氨基甲基化对应ñ -氨基甲基衍生物。研究了合成化合物的抗氧化活性及其对凝血系统某些参数的影响。
更新日期:2020-06-04
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