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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274818Generated: November 1, 2026

Triethylamine → 6-fluoro-1-(phenylsulfonyl)-3-(1-((1-(2,2,2-trifluoroethyl)piperidin-4-yl)methyl)-1H-pyrazol-4-yl)-1H-indole

https://huagongshe.com/reaction/2274818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
Reactant6-fluoro-1-(phenylsulfonyl)-3-(1-(piperidin-4-ylmethyl)-1H-pyrazol-4-yl)-1H-indoleHCID 118060635—
SolventTolueneHCID 1140—
Product6-fluoro-1-(phenylsulfonyl)-3-(1-((1-(2,2,2-trifluoroethyl)piperidin-4-yl)methyl)-1H-pyrazol-4-yl)-1H-indoleHCID 11806026484%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6-fluoro-1-(phenylsulfonyl)-3-(1-(piperidin-4-ylmethyl)-1H-pyrazol-4-yl)-1H-indole (Intermediate 21; 277 mg; 0.63 mmol), Et3N (0.40 mL; 2.87 mmol) and 2,2,2-trifluoroethyl trifluoromethanesulfonate (147 mg; 0.63 mmol) in toluene (40 mL) was stirred at 80° C. overnight. The reaction mixture was concentrated and purified by reverse phase flash chromatography to afford 275 mg (84%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-c4652ac3b33043b99f8994a7ba162731
Source noteuspto-grants-2015_09