Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 915384Erstellt: 26. Oktober 2026

Potassium Iodide → [6-[5-(4-Trifluoromethyl-phenyl)-1H-pyrazol-3-ylmethoxy]-indol-1-yl]-acetic acid tert-butyl ester

https://huagongshe.com/reaction/915384

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktCesium carbonateHCID 10796—
Edukttert-Butyl (6-hydroxy-1H-indol-1-yl)acetateHCID 69283069—
Edukt3-Chloromethyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazoleHCID 178506111—
LösungsmittelDimethylformamideHCID 6228—
Produkt[6-[5-(4-Trifluoromethyl-phenyl)-1H-pyrazol-3-ylmethoxy]-indol-1-yl]-acetic acid tert-butyl esterHCID 1784512037%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of (6-hydroxy-indol-1-yl)-acetic acid tert-butyl ester (37 mg, 0.15 mmol), 3-chloromethyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazole (43 mg, 0.16 mmol), cesium carbonate (54 mg, 0.16 mmol) and a trace of potassium iodide were suspended in N,N-dimethylformamide (4 ml). The suspension was stirred at ambient temperature for 14 h and for 4 h at 80° C. The solvent was evaporated under reduced pressure and the residue dissolved in 1 N HCl/ice water 1/1 and ethyl acetate. The layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined organic layers were washed two times with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, heptane/AcOEt) to give 5 mg (10 μmol, 7%) of the title compound as orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265149B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-9ed5a382e2e74487b457e32e74dee025
Quellennotizuspto-grants-2007_09