反应详情

A solution of (3R)-6-cyclohexyl-3-(3-methyl-1,2,4-oxadiazol-5-yl)hexanoic acid (Preparation 45) (170 mg, 0.61 mmol) in anhydrous tetrahydrofuran (2 ml) was treated with 1,1′-carbonyldiimidazole (98 mg, 0.61 mmol) and the mixture stirred at room temperature under a nitrogen atmosphere for 20 minutes. Hydroxylamine hydrochloride (42 mg, 0.61 mmol) was then added and the mixture stirred for 18 hours. The solvent was removed under reduced pressure and the residue partitioned between hydrochloric acid (0.5M) and ethyl acetate. The layers were separated and the organic phase was washed with water, dried over anhydrous sodium sulphate, filtered and solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol (98:2) to afford the title compound as an oil (82 mg).

1. stirringthe mixture stirred for 18 hours
2. customThe solvent was removed under reduced pressure
3. customthe residue partitioned between hydrochloric acid (0.5M) and ethyl acetate
4. customThe layers were separated
5. washthe organic phase was washed with water
6. dry with materialdried over anhydrous sodium sulphate
7. filtrationfiltered
8. customsolvent removed under reduced pressure
9. customThe residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol (98:2)