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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172597Generated: October 31, 2026

Potassium Carbonate → 5-chloro-6-(2,4-difluoro-benzyloxy)-3-{5-[2-(1-hydroxy-1-methyl-ethyl)-pyrimidin-4-yl]-2-methyl-phenyl}-2-methyl-3H-pyrimidin-4-one

https://huagongshe.com/reaction/2172597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-2-methylpropanimidamide hydrochlorideHCID 42614284—
Reactant5-chloro-6-(2,4-difluoro-benzyloxy)-2-methyl-3-(2-methyl-5-propynoyl-phenyl)-3H-pyrimidin-4-oneHCID 71582645—
SolventAcetonitrileHCID 6342—
Product5-chloro-6-(2,4-difluoro-benzyloxy)-3-{5-[2-(1-hydroxy-1-methyl-ethyl)-pyrimidin-4-yl]-2-methyl-phenyl}-2-methyl-3H-pyrimidin-4-oneHCID 7158240650%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of the 5-chloro-6-(2,4-difluoro-benzyloxy)-2-methyl-3-(2-methyl-5-propynoyl-phenyl)-3H-pyrimidin-4-one of Step D (20 mg, 0.05 mmol) in acetonitrile (1 mL) as added 2-hydroxy-2-methylpropionamidine HCl (9 mg, 0.07 mmol) and potassium carbonate (20 mg, 0.15 mmol) and the slurry was heated at 85° C. for eighteen hours. The reaction was returned to ambient temperature and filtered to remove excess salts. The filtrate was concentrated and purified via normal phase chromatography (ethyl acetate/heptane) to provide the title compound as a white solid (12.5 mg, 50% yield). MS (M+H): 513; 1H NMR (400 MHz, chloroform-d) δ ppm, 1.65 (s, 6H), 2.18 (s, 3H), 2.21 (s, 3H), 5.51-5.60 (m, 2H), 6.88-6.97 (m, 2H), 7.55-7.60 (m, 3H), 7.93 (s, 1H), 8.14 (d, J=8.61 Hz, 1H), 8.78 (d, J=5.09, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056110B2
Source datasetuspto-grants-2015_06
ORD IDord-a136d2f4aa4143bdbf80964a9dbd4ff1
Source noteuspto-grants-2015_06