反应详情

Sodium methoxide (10.9 ml, a 5 M methanol solution) and benzaldehyde (3.3 ml) were added to a methanol (100 ml) solution of the 1-amino-4-(methoxycarbonyl)pyridin-2(1H)-iminium 2,4,6-trimethylbenzenesulfonate (10 g) obtained in (Example 3.18) <Step 3>, and the obtained mixture was then stirred for 1 hour. Thereafter, water (5 ml) was added to the reaction solution, and the mixed solution was then stirred at 40° C. for 30 minutes. Thereafter, methanol was distilled away under reduced pressure, water (50 ml) and methyl tert-butyl ether (50 ml) were then added to the residue, followed by stirring the mixture. An organic layer was separated from a water layer, and the water layer was then washed with methyl tert-butyl ether (50 ml) again. The water layer was adjusted to pH 4 by addition of 4 N hydrochloric acid (10 ml), and a mixed solution of methylene chloride and methanol (95:5, 50 ml) was then added thereto. Insoluble substances were removed by filtration, and an organic layer was then separated from a water layer. The water layer was extracted with a mixed solution of methylene chloride and methanol (95:5, 50 ml) twice. Organic layers were then combined, and the solvent was then distilled away under reduced pressure. The obtained residue was successively triturated with methyl tert-butyl ether (50 ml) and methanol (50 ml). The obtained solid was washed with methanol (20 ml), and was then dried at 50° C. under reduced pressure, so as to obtain the title compound (3.2 g) in the form of a brown solid.

1. customobtained in (Example 3.18) <Step 3>
2. stirringthe mixed solution was then stirred at 40° C. for 30 minutes
3. distillationThereafter, methanol was distilled away under reduced pressure, water (50 ml) and methyl tert-butyl ether (50 ml)
4. additionwere then added to the residue
5. stirringby stirring the mixture
6. customAn organic layer was separated from a water layer
7. washthe water layer was then washed with methyl tert-butyl ether (50 ml) again
8. additionThe water layer was adjusted to pH 4 by addition of 4 N hydrochloric acid (10 ml)
9. additiona mixed solution of methylene chloride and methanol (95:5, 50 ml) was then added
10. customInsoluble substances were removed by filtration
11. customan organic layer was then separated from a water layer
12. extractionThe water layer was extracted with a mixed solution of methylene chloride and methanol (95:5, 50 ml) twice
13. distillationthe solvent was then distilled away under reduced pressure
14. customThe obtained residue was successively triturated with methyl tert-butyl ether (50 ml) and methanol (50 ml)
15. washThe obtained solid was washed with methanol (20 ml)
16. customwas then dried at 50° C. under reduced pressure