反应详情

A solution of 880 mg (5 mmol) of 7-methyl-3-pyrazolo[1,5-a]pyridinecarboxylic acid in 10 ml of thionyl chloride was heated under reflux for 30 minutes. Thionyl chloride was distilled off under reduced pressure and the residue was dissolved in 30 ml of methylene chloride. The resultant solution was added dropwise under ice cooling to a solution of 644 mg (5.1 mmol) of (S)-(-)-1-azabicyclo[2.2.2]octan-3-amine, which had been prepared in accordance with the procedure disclosed in Japanese Patent Application Laid-Open No. 196583/1988, in 30 ml of methylene chloride. The resultant mixture was stirred for 30 minutes under ice cooling and for additional 40 minutes at room temperature. 2N aq. NaOH solution was added to the reaction mixture and, after the mixture so obtained was stirred for 10 minutes, the organic layer was collected. Further, the water layer was extracted with methylene chloride and the extract was dried over anhydrous potassium carbonate. Methylene chloride was distilled off under reduced pressure, and the residue was purified by chromatography on a silica gel column (chloroform:methanol=10:1, 5:1). An oily substance thus obtained was dissolved in ethyl acetate. The solvent was distilled off under reduced pressure, and crystals thus obtained were washed with ether, whereby 1.2 g (4.2 mmol) of the title compound were obtained as white crystals (yield: 84.5%).

1. temperatureunder reflux for 30 minutes
2. distillationThionyl chloride was distilled off under reduced pressure
3. dissolutionthe residue was dissolved in 30 ml of methylene chloride
4. customhad been prepared in accordance with the procedure
5. customafter the mixture so obtained
6. customthe organic layer was collected
7. extractionFurther, the water layer was extracted with methylene chloride
8. dry with materialthe extract was dried over anhydrous potassium carbonate
9. distillationMethylene chloride was distilled off under reduced pressure
10. customthe residue was purified by chromatography on a silica gel column (chloroform:methanol=10:1, 5:1)
11. customAn oily substance thus obtained
12. distillationThe solvent was distilled off under reduced pressure, and crystals
13. customthus obtained
14. washwere washed with ether