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【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