Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,6-Dihydro-2H-pyran-4-boronic acid pinacol ester | HCID 11218053 | — |
| Reactant | HCID 58466183 | HCID 58466183 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58466322 | HCID 58466322 | — |
Reaction Steps
2-Fluoro-7-(2-fluoropyridin-3-yl)-3-iodo-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazol]-2′-amine (0.151 g, 0.307 mmol), 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.150 g, 0.71 mmol), tetrakis(triphenylphosphine)palladium (0.177 g, 0.153 mmol), and potassium phosphate (0.102 mL, 1.227 mmol) were suspended in dioxane (2 mL) and water (0.5 mL) and sealed in a microwave vessel under argon. The mixture was heated to 120° C. for 20 minutes. The reaction mixture was concentrated under reduced pressure and partitioned between water (80 mL) and ethyl acetate (80 mL). The organic was dried with magnesium sulfate and evaporated to dryness under reduced pressure. Purification using silica chromatography (1-4% methanol in dichloromethane gradient) gave 3-(3,6-dihydro-2H-pyran-4-yl)-2-fluoro-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazol]-2′-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883782B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-fe0c9f06dc294875bd79e7097284c6af |
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| Source note | uspto-grants-2014_11 |
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