反应详情

温度

60 °C

6-(Hydroxy(1-(phenylsulfonyl)-1H-imidazol-4-yl)methyl)-N-methyl-2-naphthamide (8.8 g, 20.88 mmol) and manganese dioxide (16.4 g, 187.9 mmol) were added to N,N-dimethylacetamide (75 mL), and the mixture was stirred at 60° C. for 9.5 hr. The insoluble material was filtered off from the reaction mixture at 60° C., and washed with DMAc (35 mL). The filtrate and washing were combined, and cooled to 40° C., water (53 mL) was added dropwise thereto, and the mixture was stirred at the same temperature for 0.5 hr or more, and then at room temperature for 1 hr or more to give crystals. The obtained crystals were collected by filtration, and washed with water (44 mL) to give wet crystals. The obtained wet crystals were dried under reduced pressure at an outside temperature of 50° C. to give crude crystals (6.3 g). Ethyl acetate (63 mL) was warmed to 40° C., and the crude crystals (6.3 g) were added thereto. The obtained mixture was warmed to 50° C., and stirred for 0.5 hr or more. 13 mL of the solvent was evaporated under reduced pressure to give a residue. The obtained residue was allowed to cool to room temperature, diisopropyl ether (53 mL) was added dropwise thereto at the same temperature, and the mixture was stirred to give crystals. The obtained crystals were collected by filtration, and washed with a mixed solvent (20 mL) of diisopropyl ether/ethyl acetate (1:1, volume ratio) to give wet crystals. The obtained wet crystals were dried under reduced pressure at an outside temperature of 50° C. to give N-methyl-6-[(1-(phenylsulfonyl)-1H-imidazol-4-yl)carbonyl]-2-naphthamide (6.2 g, 14.9 mmol). yield 72%.

1. filtrationThe insoluble material was filtered off from the reaction mixture at 60° C.
2. washwashed with DMAc (35 mL)
3. washThe filtrate and washing
4. temperaturecooled to 40° C.
5. additionwater (53 mL) was added dropwise
6. stirringthe mixture was stirred at the same temperature for 0.5 hr or more
7. customat room temperature for 1 hr or more to give crystals
8. filtrationThe obtained crystals were collected by filtration
9. washwashed with water (44 mL)
10. customto give wet crystals
11. customThe obtained wet crystals were dried under reduced pressure at an outside temperature of 50° C.
12. customto give crude crystals (6.3 g)
13. temperatureThe obtained mixture was warmed to 50° C.
14. stirringstirred for 0.5 hr or more
15. custom13 mL of the solvent was evaporated under reduced pressure
16. customto give a residue
17. temperatureto cool to room temperature
18. stirringat the same temperature, and the mixture was stirred
19. customto give crystals
20. filtrationThe obtained crystals were collected by filtration
21. washwashed with a mixed solvent (20 mL) of diisopropyl ether/ethyl acetate (1:1, volume ratio)
22. customto give wet crystals
23. customThe obtained wet crystals were dried under reduced pressure at an outside temperature of 50° C.