HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455670Generated: October 30, 2026
Potassium Carbonate → HCID 58465943, compound
https://huagongshe.com/reaction/455670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoropyridine-3-boronic acid | HCID 2783270 | — |
| Reactant | HCID 58465878 | HCID 58465878 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58465943 | HCID 58465943 | 79% |
Reaction Steps
A 250 ml RB flask was charged with (S)-7′-bromo-4′-fluoro-2′-methoxy-2,6-dihydrospiro[[1,4]oxazine-3,9′-xanthen]-5-amine (1.0 g, 2.54 mmol), PdCl2(Cy2C6H4NMe2)2 (0.126 g, 0.178 mmol) and 2-fluoropyridin-3-ylboronic acid (0.538 g, 3.81 mmol). Dioxane (12.72 mL) and potassium carbonate (1M solution) (7.63 mL, 7.63 mmol) were added, and the mixture was flushed with argon and heated to 85° C. for 30 min. The mixture was cooled to RT and diluted with EtOAc. The organic layer was separated and concentrated under reduced pressure to give a yellow foam. The residue was purified by chromatography (5-50% of EtOAc/MeOH/NH4OH 90:10:1 in EtOAc) to afford (S)-4′-fluoro-7′-(2-fluoropyridin-3-yl)-2′-methoxy-2,6-dihydrospiro[[1,4]oxazine-3,9′-xanthen]-5-amine (0.82 g, 2.003 mmol, 79% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497264B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-27bdc2eb14774e508e3fe807198e874a |
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| Source note | uspto-grants-2013_07 |
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