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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915384Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl (6-hydroxy-1H-indol-1-yl)acetateHCID 69283069—
Reactant3-Chloromethyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazoleHCID 178506111—
SolventDimethylformamideHCID 6228—
Product[6-[5-(4-Trifluoromethyl-phenyl)-1H-pyrazol-3-ylmethoxy]-indol-1-yl]-acetic acid tert-butyl esterHCID 1784512037%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265149B2
Source datasetuspto-grants-2007_09
ORD IDord-9ed5a382e2e74487b457e32e74dee025
Source noteuspto-grants-2007_09