HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511787Generated: November 4, 2026
Potassium Phosphate, Tribasic → HCID 66953575, compound
https://huagongshe.com/reaction/1511787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Benzyl azetidin-3-ylcarbamate | HCID 17750122 | — |
| Reactant | 8-Bromo-7-fluoro-2-methoxy-1,5-naphthyridine | HCID 45480320 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Product | HCID 66953575 | HCID 66953575 | 85% |
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
| 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-b88317b9b7a14fb7922fde8e412a06bd |
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| Source note | uspto-grants-2012_07 |
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