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HRID 278022作成日:2026年10月26日

4-Fluorobenzene-1,2-diamine → 5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

https://huagongshe.com/reaction/278022

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorobenzene-1,2-diamineHCID 164584—
反応物5-Formyl-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 22626786—
溶媒NitrobenzeneHCID 7416—
生成物5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 1204181125%

反応条件

温度155 °C

反応手順

A solution of 5-formyl-3-(1-methylpiperidin-4-yl)-1H-indole (0.210 g, 0.90 mmol), and 4-fluoro-o-phenylenediamine (0.112 g, 0.90 mmol), in 15 mL of nitrobenzene was heated, with stirring, at 150-160° C. for 24 hours. An additional 0.5 equivalents of the diamine was added, and heating continued for an additional 24 hours. The solution was allowed to cool to room temperature, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography (dichloromethane:methanol 10:1.5) to give the title compound (0.075 g, 25%) as an amorphous tan solid. FDMS m/e=348 (M+). EA calculated for C21H21N4F.¾ H2O: C, 69.69; H, 6.27; N, 15.48. Found: C, 69.61; H, 6.19; N, 15.17.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358972B1
出典データセットuspto-grants-2002_03
ORD IDord-d4fb135a88004116a74448d718e06f2c
出典メモuspto-grants-2002_03