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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943707Generated: November 3, 2026

Potassium Carbonate → HCID 66936637, compound

https://huagongshe.com/reaction/1943707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
ReactantFuran-3-boronic acidHCID 2734358—
Reactant7-bromo-1H,2H,3H-pyrido[2,3-b][1,4]oxazineHCID 66789061—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66936637HCID 66936637—

Reaction Steps

To 2.0 ml of acetonitrile/0.5 ml of distilled water, 7-bromo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine (80 mg, 0.372 mmol), 3-furan boronic acid (45.7 mg, 0.409 mmol), palladium acetate (8.3 mg, 0.0372 mmol), triphenylphosphine (19.5 mg, 0.0744 mmol) and potassium carbonate (102.8 mg, 0.744 mmol) were added and reacted at 100□ for 10 min using microwave (50 W) apparatus. After completion of the reaction, the mixture was extracted with ethyl acetate, and the combined organic layer was dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by preparative TLC eluting a solvent of dichloromethane:methanol=20:1. Silica gels containing the product were eluted with dichloromethane and the solvent was evaporated to obtain 7-furan-3-yl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine in oil form (18 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394792B2
Source datasetuspto-grants-2013_03
ORD IDord-8ab27137c7f7475f9c27aa0bf9012d5f
Source noteuspto-grants-2013_03