首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Regioselective reaction: synthesis and pharmacological study of Mannich bases containing ibuprofen moiety.
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Regioselective reaction: synthesis and pharmacological study of Mannich bases containing ibuprofen moiety.

机译:区域选择性反应:含有布洛芬部分的曼尼希碱的合成和药理研究。

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摘要

A series of 4-[(4-aryl)methylidene]amino-2-(substituted-4-ylmethyl)-5-{1-[4-(2-methylpropyl)p henyl]ethyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione (6) were synthesized from an arylpropionic acid namely, ibuprofen by a three-component Mannich reaction. Aminomethylation of 4-[(4-aryl)methylidene]amino-5-{1-[4-(2-methylpropyl)phenyl] ethyl}-4H-1,2,4-triazole-3-thiol (5) with formaldehyde and a secondary amine furnished this novel series of Mannich bases (6). Both Schiff bases (5) and Mannich bases (6) were well characterized on the basis of IR, NMR, mass spectral data and elemental analysis. They were screened for their anti-inflammatory, analgesic, antibacterial and antifungal activities. Some of the Mannich bases (6) carrying morpholino and N-methylpiperazino residues were found to be promising anti-inflammatory and analgesic agents.
机译:一系列4-[((4-芳基)亚甲基]氨基-2-(取代的-4-基甲基)-5- {1- [4-(2-甲基丙基)对苯基]乙基} -2,4-二氢-通过三组分曼尼希反应由芳基丙酸即布洛芬合成3H-1,2,4-三唑-3-硫酮(6)。 4-[(4-芳基)亚甲基]氨基-5- {1- [4- [2-(2-甲基丙基)苯基]乙基} -4H-1,2,4-三唑-3-硫醇(5)的氨基甲基化与甲醛和仲胺为这一新颖的曼尼希碱系列提供了便利(6)。 Schiff碱(5)和Mannich碱(6)均基于IR,NMR,质谱数据和元素分析得到了很好的表征。筛选它们的抗炎,止痛,抗菌和抗真菌活性。发现一些带有吗啉代和N-甲基哌嗪子残基的曼尼希碱(6)是有希望的抗炎和镇痛药。

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