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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199523Generated: October 31, 2026

Potassium Carbonate → 3-chloro-4-((2,4-difluoro-3-methylbenzyl)oxy)-2'-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5',6-dimethyl-2H-[1,4'-bipyridin]-2-one

https://huagongshe.com/reaction/2199523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthylacetate heptaneHCID 21899848—
Reactant3-chloro-4-hydroxy-2'-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5',6-dimethyl-2H-[1,4'-bipyridin]-2-oneHCID 86699306—
Reactant1-(Bromomethyl)-2,4-difluoro-3-methylbenzeneHCID 86699308—
Catalyst18-Crown-6HCID 28557—
SolventDimethylformamideHCID 6228—
Product3-chloro-4-((2,4-difluoro-3-methylbenzyl)oxy)-2'-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5',6-dimethyl-2H-[1,4'-bipyridin]-2-oneHCID 7176901860.5%

Reaction Steps

To a solution of 3-chloro-4-hydroxy-2′-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5′,6-dimethyl-2H-[1,4′-bipyridin]-2-one (386 mg, 1.0 mmol) in N,N-dimethylformamide (1.7 mL) was added 1-(bromomethyl)-2,4-difluoro-3-methylbenzene (243 mg, 1.1 mmol), potassium carbonate (0.35 g, 2.52 mmol) and 18-crown-6 (7 mg). The slurry was stirred at ambient temperature for 18 hours. The reaction was partitioned between ethyl acetate and water. The organic layer was washed with water and brine and dried over magnesium sulfate. The solution was concentrated in vacuo to provide a brown oil. Normal phase chromatography (ethyl acetate/heptane) provided 319 mg of the alkylated product: MS (M+H) 528.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359300B2
Source datasetuspto-grants-2016_06
ORD IDord-f8d983b88d9241aca12e35df189b8673
Source noteuspto-grants-2016_06