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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Flourophenyl methyl sulfone | HCID 69311758 | — |
| Reactant | 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-3-piperidinol hydrochloride | HCID 69312995 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[N-[1-[N-(furan-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(2-methanesulfonylphenyl)piperidin-3-ol | HCID 69315082 | 51.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342027B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-f810be6e48ca426ab0b13dc524f14462 |
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| Source note | uspto-grants-2008_03 |
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