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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511802Generated: November 4, 2026

Potassium Phosphate, Tribasic → HCID 66954743, compound

https://huagongshe.com/reaction/1511802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Cbz-aminopiperidineHCID 1514304—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Reactant8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridineHCID 45480320—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 66954743HCID 6695474321%

Reaction Conditions

Temperature85 °C

Reaction Steps

An oven-dried vial was charged with 8-bromo-7-fluoro-2-methoxy-[1,5]naphthyridine (797 mg, 3.40 mmol), palladium(II) acetate (31 mg, 0.136 mmol), DPEphos (146 mg, 0.272 mmol), K3PO4 (1.81 g, 8.50 mmol) and piperidin-4-yl-carbamic acid benzyl ester (875 mg, 3.40 mmol). The resulting mixture was purged with argon for several min. Dioxane (11 mL) was then added via syringe and the resulting suspension was purged with argon for 3 min. The mixture was then heated at 85° C. overnight. The solvent was removed in vacuo and the residue was extracted with EA/water. The org. layer was washed with brine, dried over MgSO4 and concentrated. To the resulting solid TBME and a few drops of DCM and MeOH were added and the mixture was sonicated for 5 min and filtered to afford the title intermediate as a pale yellow foam (293 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217029B2
Source datasetuspto-grants-2012_07
ORD IDord-3936f76f53ee4b55a6068437fcc2e951
Source noteuspto-grants-2012_07