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Synthesis of Some New Pyridylethylated Benzoxa(Thia)zolinones with Analgesic Activitiy

机译:具有镇痛活性的一些新型吡啶基乙氧基化苯并恶唑啉酮类化合物的合成

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Eighteen new 3-[2-(2-/4-pyridyl)ethyl]benzoxazolinone(benzothiazolinone)derivatives were synthesized by reacting 2-/4-vinylpyridine and appropriate benzoxazoliuones and benzothiazolinones.The analgesic activities of these compounds were investigated by modified Koster and hot-plate tests.Test results revealed that most of the compounds at 100 mg/kg dose levels have higher analgesic activities than acetylsalicylic acid.Compounds with bromo substituents on the phenyl ring in the 6-position of the main ring seemed to show less activity than those with fluorinated ones.Compound 6b showed remarkably high activity in the hot-plate test,although it was inactive in the Koster test.However compound 3a had statistically significant high peripheral analgesic activity at all doses compared to other compounds,although it was inactive in the hot-plate test.
机译:通过2- / 4-乙烯基吡啶与适当的苯并恶唑酮和苯并噻唑啉酮的反应合成了18种新的3- [2-(2- / 4-吡啶基)乙基]苯并恶唑啉酮(苯并噻唑啉酮)衍生物。测试结果表明,100 mg / kg剂量水平的大多数化合物具有比乙酰水杨酸更高的镇痛活性。在主环的6位苯环上带有溴取代基的化合物似乎显示出较低的活性化合物6b在热板试验中显示出很高的活性,尽管在Koster试验中没有活性。然而,与其他化合物相比,化合物3a在所有剂量下均具有统计学上显着的高外周镇痛活性,尽管它没有活性。在热板测试中。

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