反应详情

NaBH4 (1.65 g) was added portionwise to a stirred solution of 3-benzyloxycarbonylamino-4-oxo-5-(2,3,5,6-tetrafluoro-phenoxy)-pentanoic acid tert-butyl ester (21.1 g) in anhydrous THF (220 mL) at −20° C. under nitrogen. After stirring at this temperature for 3 hours, the reaction was quenched by the addition of saturated ammonium chloride solution and diluted with DCM. The organic layer was removed and the aqueous layer re-extracted with DCM. The combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated. The residue was purified by column chromatography (10%-20% ethyl acetate/hexane). The sub-title compound was obtained as a white solid (14.6 g, 73%). 1H NMR (400 MHz, CDCl3) δ 1.45 (9H, s), 2.61-2.77 (2H, m), 3.16-3.36 (1H, 2×brd d), 4.12-4.22 (2H, m), 4.30-4.33 (1H, m), 5.44-5.69 (1H, 2×d), 6.78-6.86 (1H, m), 7.35-7.36 (5H, m) ppm; 19F NMR (346 MHz, CDCl3) (proton decoupled) δ −139.87, −139.89, −139.93, −139.95, −139.98, −157.02, −157.05, −157.06, −157.08, −157.09, −157.10, −157.12; ES (+) 488.27 (M+H).

1. customthe reaction was quenched by the addition of saturated ammonium chloride solution
2. additiondiluted with DCM
3. customThe organic layer was removed
4. extractionthe aqueous layer re-extracted with DCM
5. washThe combined organic extracts were washed with brine
6. dry with materialdried (magnesium sulfate)
7. concentrationconcentrated
8. customThe residue was purified by column chromatography (10%-20% ethyl acetate/hexane)