HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021231Generated: October 27, 2026
Potassium Carbonate → {3-[2-(4-Methoxypiperidin-1-yl)pyrimidin-5-yl]phenyl}methanol
https://huagongshe.com/reaction/1021231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxypiperidine hydrochloride | HCID 11542813 | — |
| Reactant | [3-(2-Chloropyrimidin-5-yl)phenyl]methanol | HCID 86686208 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {3-[2-(4-Methoxypiperidin-1-yl)pyrimidin-5-yl]phenyl}methanol | HCID 68309818 | 91.8% |
Reaction Steps
[3-(2-Chloropyrimidin-5-yl)phenyl]methanol (200 mg) was mixed with DMF (4 ml), and 4-methoxypiperidine hydrochloride (180 mg) and potassium carbonate (500 mg) were added thereto, followed by stirring at 70° C. for 5 hours. The reaction mixture was concentrated under reduced pressure, and CHCl3 and a saturated aqueous sodium hydrogen carbonate solution were then added thereto. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain {3-[2-(4-methoxypiperidin-1-yl)pyrimidin-5-yl]phenyl}methanol (249 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08716470B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-fe25d3a2698942b98768e45f6d263fdb |
|---|
| Source note | uspto-grants-2014_05 |
|---|