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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202416Generated: November 2, 2026

Potassium Carbonate → HCID 57325410, compound

https://huagongshe.com/reaction/2202416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
Reactant2-Hydroxy-2-methylpropanimidamide hydrochlorideHCID 42614284—
ReactantHCID 67777241HCID 67777241—
SolventDimethylformamideHCID 6228—
ProductHCID 57325410HCID 5732541039%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2′-acetyl-3-chloro-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2H-1,4′-bipyridin-2-one (0.045 g, 0.11 mmol) in DMF (0.5 mL) was added N, N dimethylformamide di-tert-butyl acetal (0.04 g, 0.2 mmol) and heated at 60° C. for 2 h. The reaction mixture was concentrated in vacuo, the residue was treated with toluene (1 mL) and concentrated in vacuo. The resulting residue was dried in vacuo for 2 h, dissolved in DMF (1 mL), and potassium carbonate (0.03 g, 0.22 mmol) and 2-hydroxy-2-methylpropiamidine hydrochloride (0.02 g, 0.14 mmol) were added. This mixture was heated at 80° C. for 12 h under nitrogen and concentrated in vacuo. The residue was partitioned between water (5 mL) and ethyl acetate (15 mL). The organic phase was washed with water, dried with magnesium sulfate, and concentrated. The resulting residue was purified by silica-gel flash chromatography using 3% methanol in ethyl acetate. Appropriate fractions were combined and concentrated under reduced pressure to give 0.022 g of the title compound. ES-MS, m/z=513 (M+H) and 535 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365546B2
Source datasetuspto-grants-2016_06
ORD IDord-53c52f6a9833452fb828532579c72e72
Source noteuspto-grants-2016_06