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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392412Generated: October 26, 2026

Potassium Carbonate → 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(2-methanesulfonylphenyl)piperidin-3-ol

https://huagongshe.com/reaction/1392412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Flourophenyl methyl sulfoneHCID 69311758—
Reactant4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-3-piperidinol hydrochlorideHCID 69312995—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(2-methanesulfonylphenyl)piperidin-3-olHCID 6931508251.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the solution of 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-3-piperidinol hydrochloride (600 mg, 1.55 mmol) obtained in Step 4 and 1-flourophenyl methyl sulfone (272 g, 1.55 mmol) in 30 ml of dimethylformamide, was added potassium carbonate (500 mg). The reaction mixture was stirred overnight at about 100° C. and cooled to room temperature. The reaction mixture was diluted with 200 ml of ethyl acetate and washed with brine. The resulting organic layer was dried and concentrated on sodium sulfate. The resulting residue was purified with column chromatography to give 390 mg of the titled compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342027B2
Source datasetuspto-grants-2008_03
ORD IDord-f810be6e48ca426ab0b13dc524f14462
Source noteuspto-grants-2008_03