反应详情

4-{(3S)-3-[(tert-Butoxycarbonyl)amino]piperidin-1-yl}-3-({[6-(2,6-difluorophenyl)-5-fluoropyridin-2-yl]carbonyl}amino)-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl acetate (4.0 mg, 0.0064 mmol) was mixed with MeOH (76 μL), THF (38 μL) and 1.0 M NaOH (42 μL, 0.042 mmol). The reaction mixture was stirred at room temperature for 30 min. The organic solvents were removed under reduced pressure. The aqueous layer was diluted with aq. NH4Cl then extracted with EtOAc twice. The combined organic layers were dried, filtered and concentrated under reduced pressure to give an intermediate, which was treated with DCM (0.065 mL) and TFA (0.065 mL, 0.84 mmol). The mixture was stirred at room temperature for 30 min., then concentrated under reduced pressure. The residue was diluted with MeOH and neutralized with small amount of NH4OH. The resulting mixture was filtered and purified by preparative LC-MS (XBridge™ preparative C18 5 μm 30×10 mm OBD™ column, flow rate 60 mL/min., eluting with a gradient of MeCN and water with 0.15% NH4OH) to give two diastereoisomers of the title compound as white powders.

1. customThe organic solvents were removed under reduced pressure
2. additionThe aqueous layer was diluted with aq. NH4Cl
3. extractionthen extracted with EtOAc twice
4. customThe combined organic layers were dried
5. filtrationfiltered
6. concentrationconcentrated under reduced pressure
7. customto give an intermediate, which
8. stirringThe mixture was stirred at room temperature for 30 min.
9. concentrationconcentrated under reduced pressure
10. additionThe residue was diluted with MeOH and neutralized with small amount of NH4OH
11. filtrationThe resulting mixture was filtered
12. custompurified by preparative LC-MS (XBridge™ preparative C18 5 μm 30×10 mm OBD™ column, flow rate 60 mL/min.
13. washeluting with a gradient of MeCN and water with 0.15% NH4OH)