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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193028Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 59375395, compound

https://huagongshe.com/reaction/2193028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
Reactant1-Butoxy-9-fluorobenzo[c]-1,6-naphthyridin-6-yl trifluoromethanesulfonateHCID 59375526—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 59375395HCID 59375395—

Reaction Conditions

Temperature100 °C

Reaction Steps

1-butoxy-9-fluorobenzo[c]-1,6-naphthyridin-6-yl trifluoromethanesulfonate (1.00 g, 2.39 mmol), potassium phosphate tribasic (1.52 g, 7.17 mmol), palladium(II) acetate (0.0540 g, 0.239 mmol), and tricyclohexylphosphine (0.134 g, 0.478 mmol) were combined in pressure vessel. Toluene (20 ml), water (6.67 ml), and isopropenylboronic acid pinacol ester (0.899 ml, 4.78 mmol) were added. The resulting suspension was purged with argon (subsurface bubbling) for 10 min. The reaction mixture was stirred in a sealed pressure vessel at 100° C. for 2.5 h. After cooling the reaction mixture was diluted with EtOAc, and washed with aqueous ammonium chloride. The organic layer was dried over sodium sulfate, filtered, and concentrated to a crude residue that was adsorbed on to silica gel and purified by column chromatography on silica gel eluting with an EtOAc/hexane gradient to afford 1-butoxy-9-fluoro-6-isopropenylbenzo[c]-1,6-naphthyridine. LRMS (ESI) calc'd for (C19H19FN2O) [M+H]+, 311.1; found 311.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329722B2
Source datasetuspto-grants-2012_12
ORD IDord-320396cf77ba4409b270ba2aea83ec78
Source noteuspto-grants-2012_12