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【结 构 式】

【分子编号】44574

【品名】2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanone

【CA登记号】

【 分 子 式 】C19H23NO3

【 分 子 量 】313.39656

【元素组成】C 72.82% H 7.4% N 4.47% O 15.32%

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:(IV)

The bromination of labeled acetophenone (I) with Br2 and AlCl3 gives phenacyl bromide (II), which is condensed with N-[2-(3,4-dimethoxyphenyl)ethyl]-N-methylamine (III), yielding the 2-aminoacetophenone (IV). The reduction of (IV) with NaBH4 affords the secondary alcohol (V), which is finally cyclized by means of H2SO4 and trifluoroacetic acid to provide the target 3-benzazepine.

1 Hieble, J.P.; Wilson III, J.W.; Weinstock, J.; The chemistry and pharmacology of 3-benzazepines derivatives. Drugs Fut 1985, 10, 8, 645.
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) 10317 Acetophenone 98-86-2 C8H8O 详情 详情
(I) 44572 acetophenone C8H8O 详情 详情
(II) 10315 2-Bromo-1-phenyl-ethanone; 2-Bromo-1-phenyl-1-ethanone 70-11-1 C8H7BrO 详情 详情
(II) 44573 2-bromo-1-phenyl-1-ethanone C8H7BrO 详情 详情
(III) 18938 2-(3,4-dimethoxyphenyl)-N-methyl-1-ethanamine; N-(3,4-dimethoxyphenethyl)-N-methylamine 3490-06-0 C11H17NO2 详情 详情
(IV) 44047 2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanone C19H23NO3 详情 详情
(IV) 44574 2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanone C19H23NO3 详情 详情
(V) 44048 2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanol C19H25NO3 详情 详情
(V) 44575 2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanol C19H25NO3 详情 详情
Extended Information