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Facile Synthesis of Furobenzothiazepines

机译:呋喃苯并硫氮杂s的简便合成

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摘要

The reaction of methyl 5-(2-isocyanatophenylthio)-2-furancarboxylate 2 with N-methylpiperazine gave 5-(2-N-piperazinocarbamoylphenylthio)-2-furancarboxylate 3a. Furthermore, 4-N-methylpiperazinyl-2-methoxycarbonylfuro[2,3-b][1,5]benzothiazepine 4a was obtained by the Bischler-Napieralski reaction of 3a with phosphorus oxychloride in the present of phosphorus pentoxide. Three furobenzothiazepines could be obtained using the same method. Based on the pharmacological studies of these compounds, it was found that 4-morpholinyl-2-methoxycarbonylfuro[2,3-b][1,5]benzothiazepine 4b had anti-inflammatory activity similar to flufenamic acid.
机译:5-(2-异氰酸根合苯硫基)-2-呋喃羧酸甲酯2与N-甲基哌嗪的反应得到5-(2-N-哌嗪基氨基甲酰基苯硫基)-2-呋喃羧酸酯3a。此外,在五氧化二磷存在下,通过3a与三氯氧化磷的Bischler-Napieralski反应,获得了4-N-甲基哌嗪基-2-甲氧基羰基呋喃[2,3-b] [1,5]苯并硫氮杂44a。用相同的方法可以得到三种呋喃苯并硫氮杂pine。基于这些化合物的药理学研究,发现4-吗啉基-2-甲氧基羰基呋喃[2,3-b] [1,5]苯并噻氮平4b具有与氟芬那酸相似的抗炎活性。

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