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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478203Generated: October 30, 2026

Potassium Carbonate → 1-(1-(3-(4-Indol-3-ylpiperidyl)propyl)-3-piperidyl)-4-methoxybenzene Hydrochloride

https://huagongshe.com/reaction/478203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
Reactant1-(3-Chloropropyl)-3-(4-methoxyphenyl)piperidine hydrochlorideHCID 18001209—
SolventAcetonitrileHCID 6342—
Product1-(1-(3-(4-Indol-3-ylpiperidyl)propyl)-3-piperidyl)-4-methoxybenzene HydrochlorideHCID 1800126098.3%

Reaction Steps

To a suspended solution of 4-(3-indolyl)piperidine (48 mg, 0.24 mmol) and 1-(3-chloropropyl)-3-(4-methoxyphenyl)piperidine hydrochloride (61 mg, 0.2 mmol) in acetonitrile (13 mL) was added potassium carbonate (111 mg, 0.8 mmol), and the resulting mixture was refluxed for 12 hours. After the precipitated salt was filtered off, the filtrate was concentrated, and the resulting crude product was purified by column chromatography on a silica gel (eluent; chloroform:ammonia-saturated chloroform=10:1→3:1→1:2) to afford a free form (92 mg) of the title compound as a colorless viscous oil. After adding hydrochloric acid/methanol to a solution of the free form in methanol, the mixture was concentrated and was then freeze-dried to afford the title compound (81 mg, yield: 80%) as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642228B1
Source datasetuspto-grants-2003_11
ORD IDord-48c1da86bfff4693b205fa9e7154138b
Source noteuspto-grants-2003_11