Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Bis(adamantan-1-yl)(butyl)phosphane | HCID 11371790 | — |
| Reactant | Potassium cyclopropyltrifluoroborate | HCID 23697338 | — |
| Reactant | HCID 89456437 | HCID 89456437 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 89457119 | HCID 89457119 | 62% |
Reaction Steps
tert-butyl 2-(5-chloro-2-fluorophenyl)-4-(1-methyl-5-(4-(benzyloxycarbonylamino)azepan-1-yl)-1H-pyrazol-4-ylcarbamoyl)thiazol-5-ylcarbamate (309 mg, 0.44 mmol), potassium cyclopropyltrifluoroborate (98 mg, 0.66 mmol), palladium acetate (20.0 mg, 0.088 mmol), butyl-di-1-adamantylphosphine (50.1 mg, 0.133 mmol) and cesium carbonate (437 mg, 1.33 mmol) were charged in a 40 mL reaction vial and vacuum purged with nitrogen three times. Toluene (10.8 mL) and water (1.2 mL) were added and the mixture was heated at 105° C. for four days, monitoring with LCMS. The reaction was filtered through Celite and washed thoroughly with methanol. The filtrate was concentrated under reduced pressure and the residue was purified via flash chromatography, eluted with 0 to 100% ethyl acetate in heptane to give tert-butyl 2-(5-cyclopropyl-2-fluorophenyl)-4-(1-methyl-5-(4-(benzyloxycarbonylamino)azepan-1-yl)-1H-pyrazol-4-ylcarbamoyl)thiazol-5-ylcarbamate (192 mg, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08614206B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-f4999f4da15e4a36a279afa2240c5d3f |
|---|
| Source note | uspto-grants-2013_12 |
|---|