Bromine → HCID 86614846, compound
Reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[N:11]=[C:6]2[CH:7]=[N:8][CH:9]=[CH:10][N:5]2[N:4]=1.[Br:14]Br>C(O)C>[BrH:14].[Br:14][C:10]1[N:5]2[N:4]=[C:3]([C:2]([F:12])([F:1])[F:13])[N:11]=[C:6]2[CH:7]=[N:8][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 500 mg (2.66 mmol) of 2-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyrazine (Intermediate 7, Step C) in 2.5 mL of dry ethanol, stirred at 0° C. under protection from moisture, was treated dropwise with 0.151 mL (2.92 mmol) of bromine. After 20 minutes at 0° C., the solution was concentrated and dried to give the title compound as an orange solid. LC-MS 267, 269 (M+1).
Workup
- concentrationthe solution was concentrated
- customdried
Sources & evidence
- ORD record
- ord-e48a2703268745d3974240685fe84e94
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07625888B2
Reaction notes
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