【结 构 式】 |
【分子编号】33377 【品名】8-chloro-3-[2-(diethylamino)ethyl]-7-hydroxy-4-methyl-2H-chromen-2-one 【CA登记号】 |
【 分 子 式 】C16H20ClNO3 【 分 子 量 】309.79244 【元素组成】C 62.03% H 6.51% Cl 11.44% N 4.52% O 15.49% |
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:(III)The cyclization of 2-chlororesorcine (I) with ethyl alpha-(beta-diethylaminoethyl) acetoacetate (II) by means of p-toluenesulfonic acid and polyphosphoric acid gives 8-chloro-3-(beta-diethylaminoethyl)-4-methyl-7-hydroxycoumarin (III), which is then condensed with ethyl chloroacetate (IV) by means of K2CO3 in refluxing acetone.
【1】 Della Valle, F.; Selected process for producing monohalogenated derivatives of 7-hydroxy-coumarin. BE 0871315; DE 2846083; ES 474445; FR 2412541; FR 2412542; GB 2008109; JP 54079282; US 4296039 . |
【2】 Castaner, J.; Hillier, K.; Serradell, M.N.; Blancafort, P.; AD-6. Drugs Fut 1979, 4, 10, 701. |
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) | 33375 | 2-chloro-1,3-benzenediol | C6H5ClO2 | 详情 | 详情 | |
(II) | 33376 | ethyl 2-[2-(diethylamino)ethyl]-3-oxobutanoate | C12H23NO3 | 详情 | 详情 | |
(III) | 33377 | 8-chloro-3-[2-(diethylamino)ethyl]-7-hydroxy-4-methyl-2H-chromen-2-one | C16H20ClNO3 | 详情 | 详情 | |
(IV) | 16601 | ethyl chloroacetate; ethyl 2-chloroacetate | 105-39-5 | C4H7ClO2 | 详情 | 详情 |
Extended Information