Ammonia → 3-(Difluoromethyl)-[1,2,4]triazolo[4,3-a]pyrazine

HRID 920989

반응식

HRID 920989 반응식
FC(F)C(O)=O.[F:7][CH:8]([F:19])[C:9]([NH:11][NH:12][C:13]1[CH:18]=[N:17][CH:16]=[CH:15][N:14]=1)=O.N>>[F:7][CH:8]([F:19])[C:9]1[N:14]2[CH:15]=[CH:16][N:17]=[CH:18][C:13]2=[N:12][N:11]=1

참가 물질

3

반응 조건

온도
140 °C

실험 절차

2,2-Difluoro-N′-pyrazin-2-yl-acetohydrazide difluoroacetate 23b (2 g, 0.01 mol) was dissolved in 10 mL of polyphosphoric acid. After stirring at 140° C. for 7 hours, the reaction mixture was cooled to 50° C. and stirred for another 12 hours. The reaction mixture was poured into 50 mL of ice-water while hot, 30% aqueous ammonia was added dropwise until the pH of the reaction mixture was between 7 and 8, and the solution was extracted with ethyl acetate (30 mL×3). The organic phase was combined, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure. The resulting residue was dissolved in 30 mL of ethyl acetate and added with activated carbon. After stirring for 30 minutes, the mixture was filtered and the filtrate was concentrated under reduced pressure to obtain 3-(difluoromethyl)-[1,2,4]triazolo[4,3-a]pyrazine 23c (460 mg, yield 30%) as a yellow solid.

후처리

  1. temperaturethe reaction mixture was cooled to 50° C.
  2. stirringstirred for another 12 hours
  3. additionwas added dropwise until the pH of the reaction mixture
  4. extractionthe solution was extracted with ethyl acetate (30 mL×3)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under reduced pressure
  8. dissolutionThe resulting residue was dissolved in 30 mL of ethyl acetate
  9. additionadded with activated carbon
  10. stirringAfter stirring for 30 minutes
  11. filtrationthe mixture was filtered
  12. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5fc32f931b9e432886e0ee24ac5a4d6a
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09273052B2

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