反应详情

To a stirred solution of 0.71 g of tert-butyl [3-amino-6-methyl-2-oxo-1,2-dihydropyridinyl]-acetate (WO 97/01338) at 0° C. under a nitrogen atmosphere was added 0.60 mL cyclohexylmethanesulfonyl chloride (J. F. King et al J. Am. Chem. Soc. 114, 1743 (1992)). After stirring at room temperature for 3 hours the reaction mixture was concentrated. The residue was dissolved in ethyl acetate, washed successively with 0.1 N hydrochloric acid, water and brine, dried over sodium sulphate and concentrated. The residue was dissolved in a mixture of 0.2 mL water and 1.8 mL trifluoroacetic acid. After stirring at room temperature for 4 h, water and ethyl acetate were added. The organic layer was separated, washed twice with 0.1 N hydrochloric acid, dried over sodium sulphate and concentrated. The solid residue was washed with a cold dichloromethane/diethyl ether mixture to give 0.72 g of the title compound.

1. concentrationwas concentrated
2. dissolutionThe residue was dissolved in ethyl acetate
3. washwashed successively with 0.1 N hydrochloric acid, water and brine
4. dry with materialdried over sodium sulphate
5. concentrationconcentrated
6. dissolutionThe residue was dissolved in a mixture of 0.2 mL water and 1.8 mL trifluoroacetic acid
7. stirringAfter stirring at room temperature for 4 h
8. additionwater and ethyl acetate were added
9. customThe organic layer was separated
10. washwashed twice with 0.1 N hydrochloric acid
11. dry with materialdried over sodium sulphate
12. concentrationconcentrated
13. washThe solid residue was washed with a cold dichloromethane/diethyl ether mixture