反应详情

To a solution of (2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)amine (0.90 g, 2.95 mmol) in 20 mL of methylene chloride at ambient temperature was added trimethylaluminum (8.85 mL of a 2.0 M solution in toluene, 17.68 mmol) dropwise. The resulting solution was allowed to stir until no more gas evolution was observed (˜15 min). To this solution was added 1-[(4-methoxy)phenyl)-3-(methoxycarbonylamino)-5-(methoxycarbonyl)pyrazole (0.90 g, 2.95 mmol) in 10 mL of methylene chloride. The resulting solution was stirred at 40° C. for 16 h and then was cooled to ambient temperature and quenched by the addition of saturated aq NH4Cl. After diluting with ethyl acetate, the organic layer was washed with 10% aq HCl, saturated aq NaHCO3 and brine, dried (MgSO4), filtered through a pad of silica gel and concentrated in vacuo. The solid residue was recrystallized from hexanes/ethyl acetate to afford 1.4 g (82%) of the title compound. LRMS (ES+): 577.9 (M+H)+.

1. custom(˜15 min)
2. stirringThe resulting solution was stirred at 40° C. for 16 h
3. customquenched by the addition of saturated aq NH4Cl
4. additionAfter diluting with ethyl acetate
5. washthe organic layer was washed with 10% aq HCl, saturated aq NaHCO3 and brine
6. dry with materialdried (MgSO4)
7. filtrationfiltered through a pad of silica gel
8. concentrationconcentrated in vacuo
9. customThe solid residue was recrystallized from hexanes/ethyl acetate