Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | Bis(adamantan-1-yl)(butyl)phosphane | HCID 11371790 | — |
| Reactant | Potassium cyclopropyltrifluoroborate | HCID 23697338 | — |
| Reactant | (R)-N-((S)-1-(4-bromo-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide | HCID 86730183 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 86730188 | HCID 86730188 | 106.5% |
Reaction Steps
To a microwave vial containing a stir bar was added (R)—N—((S)-1-(4-bromo-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide (100 mg, 0.31 mmol) followed by the addition of potassium cyclopropyltrifluoroborate (459 mg, 3.10 mmol), cesium carbonate (506 mg, 1.55 mmol) and Pd(OAc)2 (7 mg, 0.03 mmol) and di(1-adamantyl)-n-butylphosphine (22 mg, 0.06 mmol), toluene (2.6 mL) and finally water (0.5 mL). The vial capped and heated by microwave irradiation for 20 min at 100° C., followed by thermal heating at 100° C. in a preheated aluminum tray for 18 hours. The reaction mixture was diluted with a saturated solution of NH4Cl. The aqueous mixture extracted with EtOAc. Organic phases combined, washed with water, brine, dried (Na2SO4), filtered and concentrated to afford a yellow crystalline of (R)—N—((S)-1-(4-cyclopropyl-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide (116 mg, 0.33 mmol, 106% yield). LCMS m/z 284.0 (M+H)+, Rt 0.90 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957068B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-867506725c25429da721aca0984f0209 |
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| Source note | uspto-grants-2015_02 |
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