【结 构 式】 |
【分子编号】59581 【品名】5-chloro-1-(4-fluorophenyl)-3-indolinol 【CA登记号】 |
【 分 子 式 】C14H11ClFNO 【 分 子 量 】263.6985832 【元素组成】C 63.77% H 4.2% Cl 13.44% F 7.2% N 5.31% O 6.07% |
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)Decarbomethoxylation of the known 3-hydroxyindole-2-carboxylate (I) in the presence of magnesium chloride in NMP at 160 C afforded indolinone (II), which was subsequently reduced with NaBH4 to the 3-hydroxy indoline (III). Dehydration of (III) by means of trifluoroacetic acid furnished indole (IV).
【1】 Bogeso, K.P.; Hyttel, J.; Sanchez, C.; Arnt, J.; Perregaard, J.; Noncataleptogenic, centrally acting dopamine D-2 and serotonin 5-HT2 antagonists within a series of 3-substituted 1-(4-fluorophenyl)-1H-indoles. J Med Chem 1992, 35, 6, 1092. |
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) | 59579 | methyl 5-chloro-1-(4-fluorophenyl)-3-hydroxy-1H-indole-2-carboxylate | C16H11ClFNO3 | 详情 | 详情 | |
(II) | 59580 | 5-chloro-1-(4-fluorophenyl)-1,2-dihydro-3H-indol-3-one | C14H9ClFNO | 详情 | 详情 | |
(III) | 59581 | 5-chloro-1-(4-fluorophenyl)-3-indolinol | C14H11ClFNO | 详情 | 详情 | |
(IV) | 59582 | 5-chloro-1-(4-fluorophenyl)-1H-indole | C14H9ClFN | 详情 | 详情 |
Extended Information