Methylamine → N-Methyl-5-((trifluoromethyl)thio)pyridin-2-amine
反応式
Cl[C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1.[CH3:13][N:14]1C(=O)CCC1.CN.C(=O)([O-])[O-].[K+].[K+]>O>[CH3:13][NH:14][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]([F:12])([F:11])[F:10])=[CH:4][N:3]=1参加物
反応条件
- 温度
- 60 °C
実験手順
To a mixture of 2-chloro-5-trifluoromethylsulfanylpyridine (1.71 g) and NMP (16 ml), 40% of aqueous methylamine solution (1.86 g) was added dropwise, and then the mixture was heated to 60° C., and stirred with heating for 2 hours. After the mixture was cooled to room temperature, potassium carbonate (1.66 g) was added thereto, and 40% of aqueous methylamine solution (1.86 g) was added dropwise. The mixture was heated to 60° C., and stirred with heating for further 2 hours. After the mixture was cooled to room temperature, water was poured, and extracted with ethyl acetate. The combined organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 1.52 g of methyl-(5-trifluoromethylsulfanylpyridine-2-yl)-amine.
後処理
- additionwas added dropwise
- temperaturewith heating for 2 hours
- temperatureAfter the mixture was cooled to room temperature
- temperatureThe mixture was heated to 60° C.
- stirringstirred
- temperaturewith heating for further 2 hours
- temperatureAfter the mixture was cooled to room temperature
- extractionextracted with ethyl acetate
- dry with materialThe combined organic layer was dried over magnesium sulfate
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-1f353d1377f24a67ac36b4b0414857db
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08853238B2
反応ノート
読み込み中…