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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478202Generated: October 30, 2026

Potassium Carbonate → HCID 18001243, compound

https://huagongshe.com/reaction/478202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidine, 1-(3-chloropropyl)-4-phenyl-, hydrochlorideHCID 203688—
Reactant3-(4-Piperidinyl)-1H-indoleHCID 702235—
SolventDimethylformamideHCID 6228—
ProductHCID 18001243HCID 1800124340%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspended solution of 4-(3-indolyl)piperidine (2.0 g, 10 mmol) and 1-(3-chloropropyl)-4-phenylpiperidine hydrochloride (3.1 g, 11.2 mmol) in DMF (60 mL) was added potassium carbonate (5.5 g, 40 mmol), and the mixture was stirred at 100° C. for 4 hours. After the precipitated salt was filtered off, the filtrate was concentrated, water (50 mL) was added to the filtrate, and the mixture was extracted with chloroform. After drying over anhydrous sodium sulfate, the chloroform layer was concentrated to afford a crude product. The crude product was purified by column chromatography on a silica gel (silica gel NH-DM 1020 produced by Fuji Silysia Chemical Ltd., eluent; chloroform) and was then recrystallized from ethyl acetate to afford a free form (1.6 g, yield: 40%) of the title compound as white crystals. After adding hydrochloric acid/methanol to a solution of the free form (1.6 g) in methanol, the mixture was concentrated and was then recrystallized from methanol/ether to afford the title compound (1.8 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642228B1
Source datasetuspto-grants-2003_11
ORD IDord-0a2cf5f9c1ef416083e1abf734d75bb4
Source noteuspto-grants-2003_11