Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59774869 | HCID 59774869 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86621972 | HCID 86621972 | — |
Reaction Steps
To a mixture of 2-oxo-4-pyridin-3-yl-2H-chromen-7-yl trifluoromethanesulfonate (6.4 g, 17.24 mmol) in DMSO (100 mL) stirred at room temperature, triethylamine (4.85 mL, 34.5 mmol) was added. The reaction was then purged twice with carbon monoxide and palladium dichloride-(dppf)-dichloromethane (2.82 g, 3.45 mmol) was added. The mixture was purged once again with carbon monoxide and the reaction was stirred overnight at 65° C. under carbon monoxide atmosphere. After cooling, the reaction was quenched by the addition of an aqueous saturated ammonium chloride solution. The aqueous layer was extracted (3×) with ethyl acetate and the combined organic extracts were dried over MgSO4, filtered and concentrated. The crude residue obtained was purified by column chromatography (acetone/CH2Cl2, 10:90). MS (+ESI) 282.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960409B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-22e9f1382fe746f4b67dbfbf14331725 |
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| Source note | uspto-grants-2011_06 |
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