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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335814Generated: October 26, 2026

Potassium Carbonate → HCID 67383055, compound

https://huagongshe.com/reaction/335814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant(5-Chloro-2-fluoro-phenyl)boronic acidHCID 3718925—
Reactant1-(2'-amino-7-bromo-5'H-spiro[chromeno[2,3-b]pyridine-5,4'-oxazole]-3-yloxy)propan-2-oneHCID 67383082—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 67383055HCID 67383055—

Reaction Conditions

Temperature80 °C

Reaction Steps

A vial charged with 5-chloro-2-fluorophenylboronic acid (0.431 g, 2.474 mmol), palladiumtetrakis (0.057 g, 0.049 mmol), potassium carbonate (0.684 g, 4.95 mmol), and 1-(2′-amino-7-bromo-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazole]-3-yloxy)propan-2-one (0.400 g, 0.990 mmol) was treated with 5 mL dioxane followed by 1 mL water. The vial was flushed with argon and was heated to 80° C. for 3 hours. The reaction mixture was diluted with EtOAc (25 mL) and dried over MgSO4. The organic layers were combined and concentrated, and the crude residue was purified by column chromatography yielding 1-(2′-amino-7-(5-chloro-2-fluorophenyl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazole]-3-yloxy)propan-2-one. MS m/z=454.0 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-90a9f01216e04a9c85c54a0825cb7e88
Source noteuspto-grants-2014_11