【结 构 式】 |
【分子编号】24967 【品名】1-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methyl-2-propanol 【CA登记号】 |
【 分 子 式 】C17H21N3O2 【 分 子 量 】299.37276 【元素组成】C 68.2% H 7.07% N 14.04% O 10.69% |
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:(III)The cyclization of the diaminoquinoline (I) with ethoxyacetic acid (II) by heating at 120 C gives the imidazoquinoline (III), which is oxidized to the 5-N-oxide (IV) by treatment with peracetic acid. Finally, compound (IV) is aminated by means of ammonium hydroxide and p-toluenesulfonyl chloride in dichloromethane.
【1】 Graul, A.; Castañer, J.; S-28463. Drugs Fut 1999, 24, 6, 622. |
【2】 Nikolaides, N.; Lindstrom, K.J. (3M Pharmaceuticals); Process for preparing quinolone amines. WO 9417043 . |
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) | 24965 | 1-[(3-amino-4-quinolinyl)amino]-2-methyl-2-propanol | C13H17N3O | 详情 | 详情 | |
(II) | 24966 | 2-ethoxyacetic acid | 627-03-2 | C4H8O3 | 详情 | 详情 |
(III) | 24967 | 1-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methyl-2-propanol | C17H21N3O2 | 详情 | 详情 | |
(IV) | 24968 | 2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-5-ium-5-olate | C17H21N3O3 | 详情 | 详情 |
Extended Information