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作为镇痛药的2,3,4,5,6,7-六氢-1,6-亚甲基-1H-3-苯并吖庚因衍生物

2,3,4,5,6,7-hexahydro-1,6-methano-1H-3-benzazonine derivatives as analgesics.

作者信息

Shiotani S, Kometani T, Mitsuhashi K

出版信息

J Med Chem. 1975 Dec;18(12):1266-7. doi: 10.1021/jm00246a023.

Abstract

10-Methoxy- (10) and 10-hydroxy-3-methyl-2,3,4,5,6,7-hexahydro-1H-3-benzazonine (11) have been synthesized from 7-methoxy-alpha-tetralone (1) via the 1-aminomethyl compound 4, which was converted to the amino acid derivative 7. Hydrogenation and cyclization of 7 afforded the lactam 9, which was reduced with LiAlH4, followed by N-methylation to give 10, from which 11 was obtained. Compounds 10 and 11 have analgetic activity, and the former was found to be comparable to codeine.

摘要

已从7-甲氧基-α-四氢萘酮(1)经由1-氨基甲基化合物4合成了10-甲氧基-(10)和10-羟基-3-甲基-2,3,4,5,6,7-六氢-1H-3-苯并吖庚因(11),该化合物4被转化为氨基酸衍生物7。7的氢化和环化得到内酰胺9,用氢化铝锂将其还原,然后进行N-甲基化得到10,从10得到11。化合物10和11具有镇痛活性,并且发现前者与可待因相当。

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