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

HRID 533674노트

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HRID 533674 반응식
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

참가 물질

6

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온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1f353d1377f24a67ac36b4b0414857db
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08853238B2

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