HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511802Generated: November 4, 2026
Potassium Phosphate, Tribasic → HCID 66954743, compound
https://huagongshe.com/reaction/1511802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4-Cbz-aminopiperidine | HCID 1514304 | — |
| Reactant | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Reactant | 8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridine | HCID 45480320 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 66954743 | HCID 66954743 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217029B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-3936f76f53ee4b55a6068437fcc2e951 |
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| Source note | uspto-grants-2012_07 |
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