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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774222Generated: November 2, 2026

Potassium tert-butoxide → HCID 86696724, compound

https://huagongshe.com/reaction/1774222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86696649HCID 86696649—
ReactantHCID 86696725HCID 86696725—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86696724HCID 8669672426%

Reaction Conditions

Temperature95 °C

Reaction Steps

Potassium 2-methylpropan-2-olate (135 mg, 1.20 mmol), tetrabutylammonium iodide (67 mg, 0.18 mmol), and a solution of 3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)butyl methanesulfonate (0.75 mmol) in anhydrous THF (15 mL) were added to a suspension of 4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (163 mg, 0.600 mmol) in anhydrous THF (5.0 mL). The resulting mixture was stirred at 95° C. under microwave irradiation for 2 hours. The reaction was quenched with water (20 mL). The mixture was further diluted with DCM. After removal of the insoluble by filtration, the filtrate was extracted with DCM. The combined organic phases were dried over Na2SO4 and concentrated. The residue was purified by Combiflash (0.5% NH3HCO3/CH3CN) to afford 1-(3-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)butyl)-4-(2-((tetrahydro-2H-pyran-4-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (80 mg, 26% yield). LCMS (ESI) m/z: 587.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09259470B2
Source datasetuspto-grants-2016_02
ORD IDord-a32466f3d6a348c5b76ee299e5e127f0
Source noteuspto-grants-2016_02