反应详情

A solution of tert-butyl (3R)-6-cyclohexyl-3-(3-{[methyl(2-pyridinylmethyl)amino]carbonyl}-1,2,4-oxadiazol-5-yl)hexanoate (Preparation 35) (527 mg, 1.12 mmol) in dichloromethane (20 ml) was treated with trifluoroacetic acid (10 ml) and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 2 hours. The solvent was removed under reduced pressure and the residue was azeotroped from toluene. The residue was dissolved in a saturated aqueous solution of sodium hydrogen carbonate (3 ml) and the pH was adjusted to pH 4 with aqueous citric acid solution (10%w/v). The aqueous phase was extracted with ethyl acetate (×2) and the combined organic layers were washed with brine, dried over anhydrous sodium sulphate, filtered and the solvent removed under reduced pressure to afford the title compound as a yellow oil (456 mg)

1. customThe solvent was removed under reduced pressure
2. customthe residue was azeotroped from toluene
3. dissolutionThe residue was dissolved in a saturated aqueous solution of sodium hydrogen carbonate (3 ml)
4. extractionThe aqueous phase was extracted with ethyl acetate (×2)
5. washthe combined organic layers were washed with brine
6. dry with materialdried over anhydrous sodium sulphate
7. filtrationfiltered
8. customthe solvent removed under reduced pressure