【结 构 式】 |
【分子编号】44048 【品名】2-[(3,4-dimethoxyphenethyl)(methyl)amino]-1-phenyl-1-ethanol 【CA登记号】 |
【 分 子 式 】C19H25NO3 【 分 子 量 】315.41244 【元素组成】C 72.35% H 7.99% N 4.44% O 15.22% |
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:(V)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