Reaction #674295
ord-a37fc8f051724aec9244c9a4b3868890
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1OtherIt was degassed again
- 2workup.ADDITIONrefilled with N2 (2 times)
- 3Temperature(heating bath) for 16 hrs
- 4TemperatureThe reaction mixture was cooled to room temperature
- 5workup.ADDITIONH2O (30 mL) was added
- 6ExtractionThe aqueous phase was extracted with EtOAc (30 mL) and DCM (3×30 mL)
- 7DryingThe combined organic phase was dried over anhydrous Na2SO4
- 8Concentrationconcentrated by evaporation in vacuo
- 9Otherto give black residue which
- 10Otherwas purified by CombiFlash (40 g silica gel column, Hexane/EtOAc)
Procedure
tert-Butyl 6-(4-bromo-1H-pyrazol-1-yl)-2-azaspiro[3.3]heptane-2-carboxylate (145 mg, 0.42 mmol) and (±)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine (268 mg, 0.63 mmol) were added to a round bottom flask. It was vacuumed and refilled with N2 (3 times). DME (2.0 mL) and a solution of Na2CO3 (2.0 M, 1.0 mL) were sequentially added. It was vacuumed and refilled with N2 (3 times). Pd(PPh3)2Cl2 (14.7 mg, 0.021 mmol) was added. It was degassed again refilled with N2 (2 times). The mixture was stirred at 90° C. (heating bath) for 16 hrs. The reaction mixture was cooled to room temperature and H2O (30 mL) was added. The aqueous phase was extracted with EtOAc (30 mL) and DCM (3×30 mL). The combined organic phase was dried over anhydrous Na2SO4, concentrated by evaporation in vacuo to give black residue which was purified by CombiFlash (40 g silica gel column, Hexane/EtOAc) to afford (±)-tert-butyl 6-(4-(6-amino-5-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-3-yl)-1H-pyrazol-1-yl)-2-azaspiro[3.3]heptane-2-carboxylate (106 mg, 45%) as a off-white solid.