Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867181Generated: November 2, 2026

Potassium Carbonate → HCID 22049896, compound

https://huagongshe.com/reaction/1867181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(Bromomethyl)-2,4-difluorobenzeneHCID 90297—
ReactantHCID 54724215HCID 54724215—
SolventDimethylformamideHCID 6228—
ProductHCID 22049896HCID 22049896—

Reaction Steps

To a room temperature solution of methyl 5-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-2-furoate (step 1) (3.19 g, 12.8 mmol) in DMF (14 mL) was added portion-wise solid N-bromosuccinimide (2.29 g, 12.9 mmol). The reaction was stirred vigorously for 1.0 h, followed by the sequential addition of K2CO3 (1.88 g, 13.6 mmol), DMF (4.0 mL), and 2,4 difluorobenzyl bromide (2.00 mL, 15.55 mmol). The resulting suspension was stirred for 9.0 hours until complete formation of desired product was seen by LCMS analysis. The reaction was then diluted with saturated brine (300 mL) and extracted with ethyl acetate (3×300 mL). The resulting organic extracts were Na2SO4 dried, filtered, and concentrated in vacuo to a residue that was subjected to SiO2 chromatography with a gradient elution using ethyl acetate/hexanes (40:60 to 60:40) to furnish a solid (3.20 mg, 55%). 1H NMR (400 MHz, d7-DMF) δ 7.78 (app q, J=8.6 Hz, 1H), 7.48 (app d, J=3.6 Hz, 1H), 7.33 (app dt, J=10.0, 2.4 Hz, 1H), 7.21 (app dt, J=8.5, 1.8 Hz, 1H), 6.92 (d, J=3.6 Hz, 1H), 6.81 (s, 1H), 5.47 (s, 2H), 3.88 (s, 3H), 2.15 (s, 3H); LC/MS C-18 column, tr=3.11 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 454 (M+H). ES-HRMS m/z 454.0117 (M+H calcd for C19H15BrF2N2O5 requires 454.0096).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629363B2
Source datasetuspto-grants-2009_12
ORD IDord-2edb076b79e848dd86cc1ce0e0e13c76
Source noteuspto-grants-2009_12