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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20990Erstellt: 24. Oktober 2026

Water → tert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylate

https://huagongshe.com/de/reaction/20990

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
Edukt1-MethylpiperazineHCID 53167—
Edukt5-Iodo-1H-indole, N-BOC protectedHCID 16125958—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
Produkttert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylateHCID 5811740528%

Reaktionsschritte

1-(tert-Butoxycarbonyl)-5-iodoindole (3.46 g, 10.1 mmol) was dissolved in toluene (45.0 mL), and the solution was added with 4-methylpiperazine (2.24 mL, 20.2 mmol), 2,2′-(diphenylphosphino)-1,1′-binaphthyl (1.26 g, 2.02 mmol), cesium carbonate (4.94 mg, 15.2 mmol) and palladium acetate (226 mg, 1.01 mmol), followed by stirring under reflux for 24 hours. The mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (chloroform/methanol=9/1) to obtain 1-(tert-butoxycarbonyl)-5-(4-methylpiperazino)indole (887 mg, 28%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-9b5aef98020e4bc380e5b6f42844c23d
Quellennotizuspto-grants-2010_06