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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278021Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/278021

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(4-Acetamidophenyl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 9841217—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
Produkt5-(4-Aminophenyl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 1204181052%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358972B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-342819bea30a409798e78fa5392a71de
Quellennotizuspto-grants-2002_03