反应详情

温度

90 °C

To a mixture of 4-(benzyloxycarbonylamino)phenylboronic acid (1.57 g, 5.79 mmol) and ((S)-1-{(S)-2-[4-(4-bromo-phenyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester (1.74 g, 3.86 mmol) in N,N-dimethylformamide (30 mL, 400 mmol) was added water (21.91 mL, 1216 mmol) and sodium bicarbonate (2.43 g, 28.96 mmol). The resulting mixture was purged with nitrogen. Tetrakis(triphenylphosphine)palladium(0) (468 mg, 0.41 mmol) was added. The reaction mixture was purged with nitrogen and then heated at 90° C. overnight. The reaction mixture was cooled to RT, diluted with methanol (10 mL), then filtered. The filtrate was concentrated and the crude product was purified by preparative HPLC to give a white solid. (1.28 g) The crude material was dissolved in methanol (40 mL) and then pumped through a continuous flow hydrogenator at 70° C. using a palladium hydroxide on carbon (20% w/w) cartridge. The resulting solution was concentrated to ˜10 mL, treated with Stratospheres™ PL-CO3 resin and stirred at room temperature for 30 min. The reaction mixture was filtered and the filtrate was concentrated to give the title compound (680 mg).

1. customThe resulting mixture was purged with nitrogen
2. customThe reaction mixture was purged with nitrogen
3. temperatureThe reaction mixture was cooled to RT
4. additiondiluted with methanol (10 mL)
5. filtrationfiltered
6. concentrationThe filtrate was concentrated
7. customthe crude product was purified by preparative HPLC
8. customto give a white solid
9. custompumped through a continuous flow hydrogenator at 70° C.
10. concentrationThe resulting solution was concentrated to ˜10 mL
11. additiontreated with Stratospheres™ PL-CO3 resin
12. filtrationThe reaction mixture was filtered
13. concentrationthe filtrate was concentrated