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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355579Generated: November 2, 2026

N-Benzoyl-4-piperidone → HCID 178479671, compound

https://huagongshe.com/reaction/1355579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzoyl-4-piperidoneHCID 90583—
ReactantHCID 178479294HCID 178479294—
SolventIsopropanolHCID 3776—
ProductHCID 178479671HCID 17847967186.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of (1R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-imidazol-2-yl)-1-ethanamine hydrochloride (1 g, 2.65 mmol) in isopropanol (15 ml) was added N-benzoyl-4-piperidone (2.64 g, 13 mmol). The solution was refluxed for about one hour and cooled to about 20° C. The solvent was removed under reduced pressure. The residue was treated with dichloromethane (30 ml) and stirred for about 30 min at about 20° C. The resulting precipitate was collected by filtration, washed with dichloromethane and diethyl ether, and dried to afford 1.2 g of the title product as the hydrochloride salt. Melting point: 240-244° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586445B1
Source datasetuspto-grants-2003_07
ORD IDord-3e0ff5be7cd149cfbd204c6d7dd67b14
Source noteuspto-grants-2003_07