【结 构 式】 |
【分子编号】40181 【品名】4-(4-methoxyphenyl)-2-butanamine; 3-(4-methoxyphenyl)-1-methylpropylamine 【CA登记号】 |
【 分 子 式 】C11H17NO 【 分 子 量 】179.26212 【元素组成】C 73.7% H 9.56% N 7.81% O 8.93% |
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:(X)The reaction of 4-(4-methoxyphenyl)-2-butylamine (X) with 3,4-dimethoxyphenylacetic acid (XI) at 200 C gives 2-(3,4-dimethoxyphenyl)-N-(4-methoxyphenyl-1-methyl-n-propyl)acetamide (XII), which is then reduced with borane in THF to yield 3,4-dimethoxy-N-[3-(4-hydroxyphenyl)-1-methylpropyl]-beta-phenylethylamine (I), which by demethylation with HBr in refluxing acetic acid.
【1】 Castaner, J.; Thorpe, P.; Dobutamine. Drugs Fut 1977, 2, 9, 579. |
【2】 Tuttle, R.R.; Mills, J. (Eli Lilly and Company); Dopamine derivatives. DE 2317710; ES 413639; FR 2182947; GB 1392674; JP 49007237 . |
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) | 40177 | N-(3,4-dimethoxyphenethyl)-4-(4-methoxyphenyl)-2-butanamine; N-(3,4-dimethoxyphenethyl)-N-[3-(4-methoxyphenyl)-1-methylpropyl]amine | C21H29NO3 | 详情 | 详情 | |
(X) | 40181 | 4-(4-methoxyphenyl)-2-butanamine; 3-(4-methoxyphenyl)-1-methylpropylamine | C11H17NO | 详情 | 详情 | |
(XI) | 40182 | 3-(3,4-dimethoxyphenyl)propionic acid | 2107-70-2 | C11H14O4 | 详情 | 详情 |
(XII) | 40183 | 3-(3,4-dimethoxyphenyl)-N-[3-(4-methoxyphenyl)-1-methylpropyl]propanamide | C22H29NO4 | 详情 | 详情 |
Extended Information