【结 构 式】 |
【药物名称】SB-237376 【化学名称】N-[3-[2-(3,4-Dimethoxyphenyl)ethylamino]propyl]-4-nitrobenzamide hydrochloride 【CA登记号】179258-62-9, 179258-59-4 (free base) 【 分 子 式 】C20H26ClN3O5 【 分 子 量 】423.90032 |
【开发单位】GlaxoSmithKline (Originator) 【药理作用】Antiarrhythmic Drugs, CARDIOVASCULAR DRUGS, Calcium Channel Blockers, Potassium Channel Blockers |
合成路线1
The reaction of 4-nitrobenzoyl chloride (I) with 3-chloropropylamine (II) by menas of triethylamine in dichloromethane gives the corresponding amide (III), which is then condensed with 2-(3,4-dimethoxyphenyl)ethylamine (IV) by means of triethylamine in refluxing dichloromethane.
【1】 Nadler, G.M.M.G.; Martin, M.J.R. (SmithKline Beecham plc); Nitro-benzamides useful as anti-arrhythmic agents. EP 0788474; FR 2726267; JP 1998508013; US 5977179; WO 9613479 . |
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) | 18941 | p-nitrobenzoyl chloride; 4-nitrobenzoyl chloride | 122-04-3 | C7H4ClNO3 | 详情 | 详情 |
(II) | 20781 | 3-chloro-1-propanamine; 3-chloropropylamine | 14753-26-5 | C3H8ClN | 详情 | 详情 |
(III) | 20782 | N-(3-chloropropyl)-4-nitrobenzamide | C10H11ClN2O3 | 详情 | 详情 | |
(IV) | 10098 | 2-(3,4-Dimethoxyphenyl)-1-ethanamine; 3,4-Dimethoxyphenethylamine; 2-(3,4-Dimethoxyphenyl)ethylamine | 120-20-7 | C10H15NO2 | 详情 | 详情 |
Extended Information