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HRID 278021作成日:2026年10月24日

5-(4-Acetamidophenyl)-3-(1-Methylpiperidin-4-yl)-1H-Indole → 5-(4-Aminophenyl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

https://huagongshe.com/ja/reaction/278021

反応式

関与物質

役割名称HCID仕込み量
反応物5-(4-Acetamidophenyl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 9841217—
溶媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
生成物5-(4-Aminophenyl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 1204181052%

反応手順

A solution of 5-(4-acetamido phenyl)-3-(1-methylpiperidin-4-yl)-1H-indole (0.150 g, 0.43 mmol) in 2 mL of ethanol and 1 mL of 1N aqueous hydrochloric acid solution was heated with stirring overnight. The mixture was allowed to cool to room temperature, solvent was removed in vacuo, and the residue was dissolved in 2N aqueous sodium hydroxide solution and ethyl acetate. The organic layer was separated, extracted with 2N aqueous sodium hydroxide solution followed by brine, dried over sodium sulfate, filtered, concentrated and purified by silica gel (flash) chromatography to give the title compound (0.068 g, 52%) as an amorphous yellow solid. FDMS m/e=305 (M+). EA calculated for C20H23N3: C, 78.65; H, 7.59; N, 13.76. Found: C, 78.42; H, 7.71; N, 13.57.

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-342819bea30a409798e78fa5392a71de
出典メモuspto-grants-2002_03