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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370270Generated: October 25, 2026

Acetonitrile → N-(1-hexylpiperidin-4-yl)xanthene-9-carboxamide

https://huagongshe.com/reaction/370270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodohexaneHCID 12527—
ReactantN-(piperidin-4-yl)xanthene-9-carboxamide hydrochlorideHCID 23283003—
SolventWaterHCID 962—
ProductN-(1-hexylpiperidin-4-yl)xanthene-9-carboxamideHCID 11794863—

Reaction Steps

60 mg of potassium carbonate and 25 ml of iodohexane were successively added to 5.0 ml of acetonitrile suspension having 50 mg of N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride, followed by reflux under heating for 4 hours. After cooled to room temperature, water was added to the reaction solution, followed by extraction with ethyl acetate and drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by preparative thin layer chromatography (Kieselgel™60F254, Art5744 produced by Merck Co.: chloroform/methanol=10/1), and 35 mg of the title compound as a white solid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140338
Source datasetuspto-grants-2000_10
ORD IDord-5d9b8530ec924490abf026fab400f5d0
Source noteuspto-grants-2000_10