Sodium Bromate → tert-butyl[(5S)-5-[(tert-butoxycarbonyl)amino]-6-{[tert-butyl(diphenyl)silyl]oxy}hexanoyl]carbamate

To a stirred solution of the material from Step 2 (339.5 g, 595 mmol) in EtOAc (1000 mL) and H2O (1400 mL) at room temperature were added sodium bromate (250 g, 1657 mmol) and ruthenium oxide hydrate (3 g, 19.86 mmol). The reaction mixture was stirred at room temperature overnight, 50% of conversion. The mixture was then heated at 55° C. overnight. Additional sodium bromate (100 g) was added and the resulting mixture was heated at 40° C. for 12 hours. Upon cooling to room temperature, the reaction mixture was filtered through celite. The filtrate was extracted with EtOAc (2×). The combined organics were then washed with aqueous sodium bisulfite and brine, and dried over MgSO4. The filtrate was treated with charcoal (Darco® G-60, Norit Americas Inc., Marshall, Tex.) and filtered through a pad of silica gel. The filtrate was concentrated in vacuo and the residue was purified by flash chromatography on silica gel using EtOAc-hexanes to yield 128 g of the title compound as a colorless viscous oil. 1H NMR (CHCl3-d): δ 7.67-7.62 (m, 4H), 7.58-7.52 (b, 1H), 7.42-7.35 (m, 6H), 4.72-4.65 (b, 1H), 3.70-3.62 (m, 2H), 3.58-3.52 (m, 1H), 2.76-2.62 (m, 2H), 1.75-1.55 (m, 2H), 1.48 (s, 9H), 1.42 (s, 9H), 1.32-1.23 (m, 2H), 1.05 (s, 9H).

1. temperatureThe mixture was then heated at 55° C. overnight
2. temperaturethe resulting mixture was heated at 40° C. for 12 hours
3. temperatureUpon cooling to room temperature
4. filtrationthe reaction mixture was filtered through celite
5. extractionThe filtrate was extracted with EtOAc (2×)
6. washThe combined organics were then washed with aqueous sodium bisulfite and brine
7. dry with materialdried over MgSO4
8. additionThe filtrate was treated with charcoal (Darco® G-60, Norit Americas Inc., Marshall, Tex.)
9. filtrationfiltered through a pad of silica gel
10. concentrationThe filtrate was concentrated in vacuo
11. customthe residue was purified by flash chromatography on silica gel

ORD 기록

ord-beeb3631bbca49f1bf462552d27f2610

출처 데이터셋

uspto-grants-2015_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US09079834B2