反应详情

To a solution of 1-tert-butoxycarbonylpiperidine-4-carboxylic acid ethyl ester (300 mg) in tetrahydrofuran (3 ml) was dropwise added a 1.5M lithium diisopropylamide-tetrahydrofuran solution (0.97 ml) at −70° C., and the mixture was stirred at the same temperature for 50 min. Then, a solution of 7-chloromethoxy-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid benzyl ester (213 mg) in tetrahydrofuran (3 ml) was dropwise added at the same temperature, and the mixture was allowed to warm to room temperature in 2 hours in stirring. After completion of the reaction, aqueous ammonium chloride solution and water were added with ice-cooling. The mixture was extracted with ethyl acetate and the extract was washed successively with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:acetone=7:1) and dried under reduced pressure to give the title compound (170 mg).

1. stirringin stirring
2. additionwere added with ice-
3. temperaturecooling
4. extractionThe mixture was extracted with ethyl acetate
5. washthe extract was washed successively with water and saturated brine
6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
7. customthe solvent was evaporated
8. customthe obtained residue was purified by silica gel column chromatography (hexane:acetone=7:1)
9. customdried under reduced pressure