Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | HCID 58368658 | HCID 58368658 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58368643 | HCID 58368643 | 28% |
Reaction Steps
A stirred mixture of 7-acetyl-5-chloroquinolin-8-yl trifluoromethanesulfonate (0.12 g, 0.34 mmol, from Example 47, Step 2), 4-piperidinemethanol (0.047 g, 0.41 mmol), palladium acetate (1.5 mg, 0068 mmol), (S)-(−)-2,2′-bs(diphenylphosphino)-1,1′-binaphthyl (6.3 mg, 0.010 mmol), and cesium carbonate (0.31 g, 0.95 mmol) in tetrahydrofuran (3 mL) was heated at 65° C. overnight. The mixture was cooled, diluted with dichloromethane and filtered. The filtrate was washed with brine, dried over MgSO4, evaporated to dryness. The residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane) to give the desired product (30 mg, 28%). LCMS calculated for C17H20ClN2O2 (M+H)+: m/z=319.1; Found: 319.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680108B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-4e8a3d0ffae64496b0db06f9c9388410 |
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| Source note | uspto-grants-2014_03 |
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