【结 构 式】 |
【分子编号】56139 【品名】1-(3-methoxyphenyl)ethylformamide 【CA登记号】 |
【 分 子 式 】C10H13NO2 【 分 子 量 】179.21876 【元素组成】C 67.02% H 7.31% N 7.82% O 17.85% |
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)The required (R)-3-methoxy-alpha-methylbenzylamine (III) was prepared from 3’-methoxyacetophenone (I) via Leuckart reaction, upon heating at 180 C with ammonium formate. The resultant formamide (II) was hydrolyzed with concentrated HCl to the racemic amine, which was then resolved using (R)-mandelic acid.
【1】 D'Ambra, T.E.; Vanwagenen, B.C.; Duff, S.R.; Nelson, W.A. (NPS Pharmaceuticals, Inc.); Method of making a benzylpropanamine. WO 9602492 . |
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) | 18792 | 3-methoxyacetophenone; 1-(3-methoxyphenyl)-1-ethanone | 586-37-8 | C9H10O2 | 详情 | 详情 |
(II) | 56139 | 1-(3-methoxyphenyl)ethylformamide | C10H13NO2 | 详情 | 详情 | |
(III) | 56140 | (R)-1-(3-Methoxyphenyl)ethylamine; (R)-3-Methoxy-alpha-methylbenzylamine; (R)-m-Methoxy-alpha-methylbenzylamine | 88196-70-7 | C9H13NO | 详情 | 详情 |
Extended Information