【结 构 式】 |
【分子编号】28756 【品名】ethyl 2-(2,3-dihydro-1,4-benzodioxin-2-yl)ethanimidoate 【CA登记号】 |
【 分 子 式 】C12H15NO3 【 分 子 量 】221.25604 【元素组成】C 65.14% H 6.83% N 6.33% O 21.69% |
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 partial alcoholysis of 2-cyanomethyl-1,4-benzodioxane (I) with ethanol and HCl in ether gives ethyl-(1,4-benzodioxan-2-yl)acetimidate (II), which is cyclized with aminoacetaldehyde diethylketal (III) in refluxing ethanol yielding 2-[(1,4-benzodioxan-2-yl)methyl]imidazole (IV). Finally, this compound is alkylated with ethyl iodide (V) and NaH in DMF.
【1】 Caroon, J.M.; et al.; Structure-activity relationships for 2-substituted imidazoles as alpha2-adrenoceptor antagonists. J Med Chem 1982, 25, 6, 666-670. |
【2】 Kluge, A.F.; Strosberg, A.M.; Whiting, R.; Christie, G. (Syntex (USA), Inc.); 2-(1,4-Benzodioxan-2-ylalkyl)miidazoles useful as antidepressants. EP 0047531; JP 57050989; US 4302469 . |
【3】 Castaner, J.; Serradell, M.N.; Imiloxan. Drugs Fut 1986, 11, 2, 108. |
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) | 28755 | 2-(2,3-dihydro-1,4-benzodioxin-2-yl)acetonitrile | C10H9NO2 | 详情 | 详情 | |
(II) | 28756 | ethyl 2-(2,3-dihydro-1,4-benzodioxin-2-yl)ethanimidoate | C12H15NO3 | 详情 | 详情 | |
(III) | 10331 | 2,2-Diethoxy-1-ethanamine; 2,2-Diethoxyethylamine; Aminoacetaldehyde diethyl acetal | 645-36-3 | C6H15NO2 | 详情 | 详情 |
(IV) | 28757 | 2-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-1H-imidazole | C12H12N2O2 | 详情 | 详情 | |
(V) | 28758 | 1-iodopropane | 107-08-4 | C3H7I | 详情 | 详情 |
Extended Information