反应详情

To a stirred solution of 1-(5-((tert-butyldiphenylsilyloxy)methyl)-4-((2R,6S)-2,6-dimethylmorpholino)-3-fluoro-2-(propan-2-ylideneaminooxy)phenyl)ethanone (Intermediate 32, 77 mg, 0.13 mmol, crude reaction product from above reaction) dissolved in ethanol (5 ml) was treated with 5 ml of 5% aqueous HCl at 75° C. for 2 hours. Reaction quenched with 10% aqueous sodium bicarbonate solution and extracted with EtOAc. The organic layer washed with water, dried, and concentrated. The residue purified over a silica gel flash column (elution with 50-70% EtOAc in hexanes) to give the title compound (15 mg, 39%).

1. customfrom above reaction)
2. customReaction
3. customquenched with 10% aqueous sodium bicarbonate solution
4. extractionextracted with EtOAc
5. washThe organic layer washed with water
6. customdried
7. concentrationconcentrated
8. customThe residue purified over a silica gel flash column (elution with 50-70% EtOAc in hexanes)