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【结 构 式】

【分子编号】25648

【品名】3-[3-(1-piperazinyl)propyl]-5-(4H-1,2,4-triazol-4-yl)-1H-indole

【CA登记号】

【 分 子 式 】C17H22N6

【 分 子 量 】310.40212

【元素组成】C 65.78% H 7.14% N 27.07%

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:(V)

Alkylation of N-Boc-piperazine (I) with bromoacetal (II) provided piperazine acetal (III). This was submitted to Fisher cyclization with 4-(1,2,4-triazol-4-yl)phenyl hydrazine (IV) in aqueous H2SO4 to afford the deprotected indole (V). Wittig reaction of 3-fluorobenzaldehyde (VII) with phosphorane prepared from (methoxymethyl)phosphonium salt (VI) and PhLi furnished the methoxyvinyl compound (VIII) as an E:Z mixture. Subsequent acid hydrolysis of the enol ether function of (VIII) yielded aldehyde (IX). The target compound was then obtained by reductive alkylation of piperazine (V) with aldehyde (IX) in the presence of NaBH3CN.

1 Chambers, M.S.; Goodacre, S.; Street, L.J.; et al.; 3-(Piperazinylpropyl)indoles: Selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agents. J Med Chem 1999, 42, 4, 691.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VIIIa) 25650 1-fluoro-3-[(E)-2-methoxyethenyl]benzene; (E)-2-(3-fluorophenyl)ethenyl methyl ether C9H9FO 详情 详情
(VIIIb) 53875 (Z)-2-(3-fluorophenyl)ethenyl methyl ether; 1-fluoro-3-[(Z)-2-methoxyethenyl]benzene n/a C9H9FO 详情 详情
(I) 13225 N-tert-Butoxycarbonyl piperazine; tert-butyl 1-piperazinecarboxylate;tert-butyl piperazine-1-carboxylate 143238-38-4 C9H18N2O2 详情 详情
(II) 25645 5-bromo-1-methoxypentyl methyl ether; 5-bromo-1,1-dimethoxypentane C7H15BrO2 详情 详情
(III) 25646 tert-butyl 4-(5,5-dimethoxypentyl)-1-piperazinecarboxylate C16H32N2O4 详情 详情
(IV) 25647 4-(4-hydrazinophenyl)-4H-1,2,4-triazole C8H9N5 详情 详情
(V) 25648 3-[3-(1-piperazinyl)propyl]-5-(4H-1,2,4-triazol-4-yl)-1H-indole C17H22N6 详情 详情
(VI) 25649 (methoxymethyl)(triphenyl)phosphonium bromide C20H20BrOP 详情 详情
(VII) 18887 3-Fluorobenzaldehyde 456-48-4 C7H5FO 详情 详情
(IX) 25651 3-(3-fluorophenyl)propanal C9H9FO 详情 详情
Extended Information