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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511787Generated: November 4, 2026

Potassium Phosphate, Tribasic → HCID 66953575, compound

https://huagongshe.com/reaction/1511787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBenzyl azetidin-3-ylcarbamateHCID 17750122—
Reactant8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridineHCID 45480320—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
ProductHCID 66953575HCID 6695357585%

Reaction Conditions

Temperature85 °C

Reaction Steps

An oven-dried vial was charged with 8-bromo-7-fluoro-2-methoxy-[1,5]naphthyridine (commercial; 2.0 g, 7.78 mmol), palladium(II) acetate (70 mg, 0.31 mmol), DPEphos (335 mg, 0.62 mmol), K3PO4 (4.13 g, 19.45 mmol) and azetidin-3-yl-carbamic acid benzyl ester (1.68 g, 8.17 mmol). The resulting mixture was purged with argon for several min. Dioxane (25 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 beige solid (2.53 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217029B2
Source datasetuspto-grants-2012_07
ORD IDord-b88317b9b7a14fb7922fde8e412a06bd
Source noteuspto-grants-2012_07