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Synthesis and analgesic activity of some 1-benzofurans, 1-benzothiophenes and indoles

机译:某些1-苯并呋喃,1-苯并噻吩和吲哚的合成和镇痛活性

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3-Unsubstituted 1-benzofurans 1e and 1f, 3-methyl-1-benzofurans 1a-1d, and 3-amino-1-benzofurans 2a-2l, as well as 3-amino-1-benzothiophenes aa, 3b and 3-aminoindoles 4a-4f 11a, and 11b were prepared and tested as analgesics. The 3-amino-1-benzofurans 2 were prepared from the corresponding 2-hydroxybenzonitriles 5 and phenacyl bromides 6 via intermediates 7. Similar treatment df 2-sulfanlylbenzonitrile (8) provided 3-amino-1-benzothiophenes 3. appropriately substituted 2-aminobenzonitriles 9 then provided N-substituted 3-aminoindoles 4. 1-(Ethoxycarbonyl)indoles 4e and 4f were successfully deprotected giving indoles 11a and 11b, respectively. [References: 30]
机译:3-未取代的1-苯并呋喃1e和1f,3-甲基-1-苯并呋喃1a-1d和3-氨基-1-苯并呋喃2a-2l以及3-氨基-1-苯并噻吩aa,3b和3-氨基吲哚制备4a-4f 11a和11b并作为止痛药进行测试。通过中间体7由相应的2-羟基苯甲腈5和苯甲酰溴6制备3-氨基-1-苯并呋喃2。类似的处理,由df 2-硫烷基苯甲腈(8)提供3-氨基-1-苯并噻吩3。适当取代的2-氨基苯甲腈然后,图9提供了N-取代的3-氨基吲哚4。1-(乙氧羰基)吲哚4e和4f被成功地去保护,分别得到吲哚11a和11b。 [参考:30]

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