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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108210Generated: October 26, 2026

Potassium Iodide → 5-Fluoro-3-(1-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl}piperidin-4-ylmethyl)-1H-indole

https://huagongshe.com/reaction/1108210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazineHCID 595673—
Reactant5-fluoro-3-[(4-piperidinyl)methyl]-1H-indoleHCID 11287716—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-Fluoro-3-(1-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl}piperidin-4-ylmethyl)-1H-indoleHCID 982571476%

Reaction Steps

Pulverized potassium carbonate (0.33 g, 2.4 mmole) and potassium iodide (0.40 g, 2.4 mmole) was added to a mixture of 4-(5-fluoro-1H-indol-3-yl)methylpiperidine (0.5 g, 2.3 mmole) and 1-(2-chloroethyl)-4-(2-methoxyphenyl)piperazine (0.58 g, 2.3 mmole) in 20 ml of acetonitrile. The resulting mixture was heated to reflux under nitrogen for 3 hours. After cooling, it was diluted with water (150 ml) and the product extracted into ethyl acetate (50 ml). The organic layer was washed with water (50 ml), brine (50 ml), and after drying over sodium sulfate, filtration and concentration in vacuo afforded the required product as a white solid (0.78 g, 76%). Treatment with an excess of 0.25M ethanolic fumaric acid solution gave the acid addition salt, which was recrystallized from ethanol/diethyl ether to afford the title product as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066637
Source datasetuspto-grants-2000_05
ORD IDord-5e0f2841f09c4f7ea002ca9e5f0ee84c
Source noteuspto-grants-2000_05