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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431448Generated: November 3, 2026

Sodium Carbonate → HCID 59631138, compound

https://huagongshe.com/reaction/1431448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-5,7-difluoro-3-methyl-2-(pyridin-2-yl)quinolineHCID 59631025—
ReactantHCID 59631200HCID 59631200—
SolventDimethylformamideHCID 6228—
ProductHCID 59631138HCID 59631138—

Reaction Conditions

Temperature0 °C

Reaction Steps

A dry flask containing 5-bromo-2-(3,6-dihydro-2H-pyran-4-yl)-3-pyridinamine (0.17 g, 0.67 mmol) in dry DMF (5.0 mL) was cooled to 0° C., then sodium hydride, 60% dispersion in mineral oil (54.9 mg, 1.37 mmol) was added carefully in portions. The mixture was stirred at 0° C. for 15 min, then 4-chloro-5,7-difluoro-3-methyl-2-(2-pyridinyl)quinoline (0.22 g, 0.74 mmol) was added in portions. Upon complete addition, the mixture was warmed to 60° C. After 18 h, the reaction was cooled to rt then was carefully treated with 10% sodium carbonate solution. The black mixture was subsequently extracted five times with DCM:MeOH (90:10). The organic extraction was then washed one time with brine and dried over anhydrous magnesium sulfate. After filtration and concentration, the brownish residue was treated with isopropanol and warmed to 45° C. After 30 min, the solid was filtered and rinsed twice with MeOH to afford a tan solid as mostly N-(5-bromo-2-(3,6-dihydro-2H-pyran-4-yl)-3-pyridinyl)-5,7-difluoro-3-methyl-2-(2-pyridinyl)-4-quinolinamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-1314821cac2a46188f8b9883eaa25630
Source noteuspto-grants-2015_01