Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516983Generated: October 29, 2026

Potassium Carbonate → 2'-Acetyl-3-chloro-4-(3,5-difluoro-pyridin-2-ylmethoxy)-5'-methyl-[1,4']bipyridinyl-2-one

https://huagongshe.com/reaction/516983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)-3,5-difluoropyridineHCID 53403744—
Reactant2'-Acetyl-3-chloro-4-hydroxy-5'-methyl-[1,4]bipyridinyl-2-oneHCID 117729626—
Catalyst18-Crown-6HCID 28557—
SolventDimethylformamideHCID 6228—
Product2'-Acetyl-3-chloro-4-(3,5-difluoro-pyridin-2-ylmethoxy)-5'-methyl-[1,4']bipyridinyl-2-oneHCID 117729530—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2′-acetyl-3-chloro-4-hydroxy-5′-methyl-[1,4′]bipyridinyl-2-one of part D (500 mg, 1.7 mmol) in N,N-dimethylformamide (3 mL) was added 2-chloromethyl-3,5-difluoro-pyridine (277 mg, 1.7 mmol), potassium carbonate (590 mg, 4.28 mmol) and 18-crown-6 (10 mg) and the reaction was stirred at 60° C. for 4 h. After cooling the solution was partitioned between ethyl acetate and water. The organic layer was washed with water and brine and dried over magnesium sulfate. The solution was filtered and concentrated in vacuo. The crude material was purified using normal phase chromatography (ethyl acetate/heptane) to provide alkylated product as a yellow solid (397 mg): MS (ES) m/e 420 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115089B2
Source datasetuspto-grants-2015_08
ORD IDord-90c3921b347b445b9224ee3d0a6ce4da
Source noteuspto-grants-2015_08