【结 构 式】 |
【分子编号】34398 【品名】4-chloro-2-(2-naphthyl)quinoline 【CA登记号】 |
【 分 子 式 】C19H12ClN 【 分 子 量 】289.76372 【元素组成】C 78.76% H 4.17% Cl 12.24% N 4.83% |
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:(I)The condensation of 4-chloro-2-(2-naphthyl)quinoline (I) with p-aminophenol (II) at 130 C provided the corresponding 4-anilinoquinoline (III). Then, Mannich reaction of (III) with N-methylpiperazine (IV) and formaldehyde furnished the title compound.
【1】 Kotecka, B.M.; Strekowski, L.; Say, M.; Manzel, L.; Henary, M.; Zegrocka, O.; Macfarlane, D.E.; Mokrosz, M.J.; Structure-activity relationship analysis of substituted 4-quinolinamines, antagonists of immunostimulatory CpG-oligodeoxynucleotides. Bioorg Med Chem Lett 1999, 9, 13, 1819. |
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) | 34398 | 4-chloro-2-(2-naphthyl)quinoline | C19H12ClN | 详情 | 详情 | |
(II) | 15715 | 4-Aminophenol | 123-30-8 | C6H7NO | 详情 | 详情 |
(III) | 34399 | 4-[[2-(2-naphthyl)-4-quinolinyl]amino]phenol | C25H18N2O | 详情 | 详情 | |
(IV) | 10061 | 1-Methylpiperazine; 1-Methyl piperazine; N-Methylpiperazine | 109-01-3 | C5H12N2 | 详情 | 详情 |
Extended Information