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Ammonium Hydroxide → 2-(Trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrazine

HRID 1454798
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HRID 1454798 반응식
[F:1][C:2]([F:14])([F:13])[C:3](=[N:11]O)[NH:4][C:5]1[CH:10]=[N:9][CH:8]=[CH:7][N:6]=1.[OH-].[NH4+]>>[F:1][C:2]([F:14])([F:13])[C:3]1[N:4]=[C:5]2[CH:10]=[N:9][CH:8]=[CH:7][N:6]2[N:11]=1
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참가 물질

3

반응물 2

HCID 14923Ammonium HydroxideHCID 178526369HCID 178526369, 화합물

생성물 1

HCID 533933572-(Trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrazine

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온도
150 °C

실험 절차

A mixture of 2,2,2-trifluoro-N′-hydroxy-N-pyrazin-2-ylethanimidamide (10.5 g, 50.97 mmol, from Step B) and polyphosphoric acid (80 mL) was heated to 150° C. with stirring for 18 h. The solution was added to ice and neutralized by addition of ammonium hydroxide. The dark aqueous solution was extracted three times with ethyl acetate, washed with brine, and dried over anhydrous magnesium sulfate. Concentration followed by flash chromatography (50% then 100% ethyl acetate/hexane) afforded the title compound as a yellow solid. 1H-NMR (500 MHz, CDCl3): δ 8.42 (d, 1H, J=4.6 Hz), 8.67 (dd, 1H, J=1.4 and 4.6 Hz), 9.47 (d, 1H, J=1.4 Hz). LC/MS 189 (M+1).

후처리

  • additionThe solution was added to ice
  • extractionThe dark aqueous solution was extracted three times with ethyl acetate
  • washwashed with brine
  • dry with materialdried over anhydrous magnesium sulfate
  • concentrationConcentration
  • 출처 및 근거

    ORD 기록
    ord-13c09cadc3e24acba63dc696f53e0aea
    출처 데이터셋
    uspto-grants-2009_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07482336B2

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