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

HRID 1158770
Notes
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Reaction equation

HRID 1158770 reaction equation
[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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 14923Ammonium HydroxideHCID 178526369HCID 178526369, compound

Product 1

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

Conditions

Temperature
150 °C

Procedure

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.

Workup

  • 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
  • Sources & evidence

    ORD record
    ord-cfccef9001fc4619b4044565dd221700
    Source dataset
    uspto-grants-2010_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07812027B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes