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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356390Generated: November 3, 2026

Potassium Iodide → 2-Ethyl-6-fluoro-3-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-YL}-1-phenyl-1H-indole

https://huagongshe.com/reaction/2356390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-[(3-bromopropyl)thio]-4-fluoro-HCID 14575314—
Reactant2-Ethyl-6-fluoro-1-phenyl-3-piperidin-4-YL-1H-indoleHCID 58748000—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Ethyl-6-fluoro-3-{1-[3-(4-fluorophenylsulfanyl)-propyl]-piperidin-4-YL}-1-phenyl-1H-indoleHCID 1195252464%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-ethyl-6-fluoro-1-phenyl-3-piperidin-4-yl-1H-indole (70 mg, TFA salt), 1-(3-Bromo-propylsulfanyl)-4-fluoro-benzene (44 mg), potassium iodide (5 mg) and potassium carbonate (55 mg) in DMF (3 ml) is heated at 80° C. for 3 h, and allowed to cool to r.t. overnight. Ethyl acetate (50 ml) and water (25 ml) are added and the organic phase is washed with water, dried and concentrated in vacuo. The crude product is purified by flash chromatography (98:2 CH2Cl2:MeOH) to give 50 mg pure product (64%) as brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759365B2
Source datasetuspto-grants-2010_07
ORD IDord-f02b3860461d421696049fe42406db5c
Source noteuspto-grants-2010_07