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【结 构 式】

【分子编号】18588

【品名】2-(1-naphthyl)-1-ethanamine hydrochloride

【CA登记号】

【 分 子 式 】C12H14ClN

【 分 子 量 】207.7026

【元素组成】C 69.39% H 6.79% Cl 17.07% N 6.74%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(II)

Reduction of 1-naphthylacetonitrile (1) by catalytic hydrogenation using Raney Nickel in a NH3 saturated EtOH solution afforded 2-(1-naphthyl)ethylamine, which was then converted to hydrochloride salt (II). Further condensation with cyclobutanecarbonyl chloride (III) in the presence of K2CO3 provided the target amide.

1 Leclerc, V.; Fourmaintraux, E.; Depreux, P.; Lesieur, D.; Morgan, P.; Howell, H.E.; Renard, P.; Caignard, D.H.; Pfeiffer, B.; Delagrange, P.; Guardiola-Lemaitre, B.; Andrieux, J.; Synthesis and structure-activity relationships of novel naphthalenic and bioisosteric related amidic derivatives as melatonin receptor ligands. Bioorg Med Chem 1998, 6, 10, 1875.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 18587 2-(1-naphthyl)acetonitrile 132-75-2 C12H9N 详情 详情
(II) 18588 2-(1-naphthyl)-1-ethanamine hydrochloride C12H14ClN 详情 详情
(III) 18589 cyclobutanecarbonyl chloride 5006-22-4 C5H7ClO 详情 详情
Extended Information