Köksal Meriç, Gökhan Nesrin, Küpeli Esra, Yesilada Erdem, Erdoğan Hakki
Yeditepe University, Faculty of Pharmacy, Istanbul, Turkey.
Arch Pharm (Weinheim). 2005 Mar;338(2-3):117-25. doi: 10.1002/ardp.200400937.
The synthesis of a novel series of Mannich bases of 5-/6-acyl-5-methyl-2-benzoxazolinones has been described. The structures attributed to compounds 2a, 3a, 4a, 4b, 9a, 9b, 5a-5g, 6a-6g, 10a, 10g, 11a, 11g have been elucidated using IR and (1)H NMR spectroscopic techniques besides elemental analysis. The compounds have been evaluated for their in vivo analgesic and antiinflammatory activities using the p-benzoquinone-induced writhing test and the carrageenan hind paw oedema test in mice, respectively. In addition, the ulcerogenic effects of the compounds were determined. Among the tested derivatives most promising results were obtained for the compounds bearing a 6-(4-chlorobenzoyl) at C-6 position and 2-/4-fluorophenyl at C-3 position of 2-benzoxazolinone ring (11c, 11d).
已描述了一系列新型的5-/6-酰基-5-甲基-2-苯并恶唑啉酮曼尼希碱的合成。除元素分析外,还使用红外光谱和(1)H核磁共振光谱技术阐明了化合物2a、3a、4a、4b、9a、9b、5a-5g、6a-6g、10a、10g、11a、11g的结构。分别使用对苯醌诱导的扭体试验和角叉菜胶致小鼠后爪水肿试验对这些化合物的体内镇痛和抗炎活性进行了评估。此外,还测定了这些化合物的致溃疡作用。在测试的衍生物中,2-苯并恶唑啉酮环C-6位带有6-(4-氯苯甲酰基)且C-3位带有2-/4-氟苯基的化合物(11c、11d)获得了最有前景的结果。