反応式
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[C:4]([Br:9])[N:3]=1.[C:10]([O-])([O-])=O.[K+].[K+].CI.O>CS(C)=O>[Br:1][C:2]1[C:7]([O:8][CH3:10])=[CH:6][CH:5]=[C:4]([Br:9])[N:3]=1参加物
6
実験手順
To a solution of 52.5 g 2,6-dibromopyridin-3-ol (example E1) in 90 ml DMSO were added 26.2 g K2CO3 and 43.8 ml methyl iodide and the reaction mixture was stirred under reflux for one hour. The mixture was allowed to cool down to room temperature and poured into 1 l of water and stirred for 3 h at 80° C. After cooling to room temperature the resulting solid was filtered, the filter cake was washed with ice cold water and dried under vacuum to yield the title compound.
後処理
- temperatureunder reflux for one hour
- stirringstirred for 3 h at 80° C
- temperatureAfter cooling to room temperature the resulting solid
- filtrationwas filtered
- washthe filter cake was washed with ice cold water
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-e5beefebb0a44d4eaeed350d335a5d50
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08273890B2
関連ノート
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