Methylamine → N-Methyl-5-((trifluoromethyl)thio)pyridin-2-amine

HRID 533674ノート

反応式

HRID 533674 の反応式
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

6

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

  1. additionwas added dropwise
  2. temperaturewith heating for 2 hours
  3. temperatureAfter the mixture was cooled to room temperature
  4. temperatureThe mixture was heated to 60° C.
  5. stirringstirred
  6. temperaturewith heating for further 2 hours
  7. temperatureAfter the mixture was cooled to room temperature
  8. extractionextracted with ethyl acetate
  9. dry with materialThe combined organic layer was dried over magnesium sulfate
  10. 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

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