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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20991Erstellt: 24. Oktober 2026

Water → 1-(Tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indole

https://huagongshe.com/de/reaction/20991

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN,N-DimethylpropargylamineHCID 81643—
Edukt5-Iodo-1H-indole, N-BOC protectedHCID 16125958—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDiethylamineHCID 8021—
Produkt1-(Tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indoleHCID 6849342990%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

1-(tert-Butoxycarbonyl)-5-iodoindole (1.00 g, 2.91 mmol) was dissolved in diethylamine (20 mL), and the solution was added with bis(triphenylphosphine)dichloropalladium (163 mg, 0.233 mmol), cuprous iodide (44.4 mg, 0.233 mmol) and 1-dimethylamino-2-propyne (0.628 mL, 5.82 mmol), followed by stirring at 80° C. for 7.0 hours. The reaction 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 preparative thin-layer chromatography (chloroform/methanol=19/1) to obtain 1-(tert-butoxycarbonyl)-5-(3-dimethylamino-2-propyn-1-yl)indole (0.78 g, yield 90%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a8a7964606714175a8ec31928416e35e
Quellennotizuspto-grants-2010_06