Synthesis and pharmacological properties of derivatives of alpha-amino-beta-(p-chlorobenzoyl)-propionic acid and alpha-amino-gamma-(p-chlorophenyl)-tetrahydrofuran-2-one.

R Zabska, T Jakóbiec, R Dobek, M Wilimowski, J Barczyńska, L Kedzierska-Goździk, W Wojewódzki, M Rutkowska, E Duś, A Szelag
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Abstract

Several new alpha-aminoderivatives of gamma-(p-chlorophenyl)-tetrahydrofuran-2-one were synthesized. alpha-Aminoderivatives of beta-(p-chlorobenzoyl)-propionic acid 2-13 were used as the substrates. After the reduction with NaBH4 at 10-12 degrees C and cyclization the compounds were converted into the appropriate derivatives of tetrahydrofuran-2-one 16-26. In pharmacological tests compounds 9 and 26 abolished the aggressiveness in isolated mice while compound 8 showed antiinflammatory activity.

α -氨基-(对氯苯甲酰)-丙酸和α -氨基-(对氯苯甲酰)-四氢呋喃-2-酮衍生物的合成及药理性质。
合成了几种新的-(对氯苯基)-四氢呋喃-2- 1的α -氨基衍生物。以-(对氯苯甲酰)-丙酸2-13的α -氨基衍生物为底物。经过10-12℃NaBH4还原和环化后,化合物转化为相应的四氢呋喃-2- 1 - 16-26衍生物。药理实验表明,化合物9和26能消除离体小鼠的侵袭性,而化合物8具有抗炎活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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