Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methoxypiperidine hydrochlorideHCID 11542813—
Reactant[3-(2-Chloropyrimidin-5-yl)phenyl]methanolHCID 86686208—
SolventDimethylformamideHCID 6228—
Product{3-[2-(4-Methoxypiperidin-1-yl)pyrimidin-5-yl]phenyl}methanolHCID 6830981891.8%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-fe25d3a2698942b98768e45f6d263fdb
Source noteuspto-grants-2014_05