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【结 构 式】

【分子编号】18669

【品名】1-(4-bromo-1-phenylbutyl)benzene

【CA登记号】

【 分 子 式 】C16H17Br

【 分 子 量 】289.21498

【元素组成】C 66.45% H 5.92% Br 27.63%

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)

Alkylation of 5-hydroxyisoquinoline (I) with bromide (II) in DMF at 80 C afforded isoquinolinium salt (III). This was reduced to tetrahydroisoquinoline (IV) by catalytic hydrogenation in the presence of Pd/C. Finally, Mannich reaction with formaldehyde and perhydroazepine (V) in THF-water at r.t. provided the target compound.

1 Yuen, P.; Schelkun, R.M.; Szoke, B.; Tarczy-Hornoch K.; Synthesis and structure-activity relationship of substituted 1,2,3,4-tetrahydroisoquinolines as N-type calcium channel blockers. Bioorg Med Chem Lett 1998, 8, 18, 2415.
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) 18668 5-isoquinolinol 2439-04-5 C9H7NO 详情 详情
(II) 18669 1-(4-bromo-1-phenylbutyl)benzene C16H17Br 详情 详情
(III) 18670 2-(4,4-diphenylbutyl)-5-hydroxyisoquinolinium bromide C25H24BrNO 详情 详情
(IV) 18671 2-(4,4-diphenylbutyl)-1,2,3,4-tetrahydro-5-isoquinolinol C25H27NO 详情 详情
(V) 18672 azepane 111-49-9 C6H13N 详情 详情
Extended Information