Bromine → HCID 23510323, compound
Reaction equation
[CH3:1][C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH2:12])[CH:8]=2)[N:3]=1.[Br:13]Br>C(O)(=O)C>[BrH:13].[CH3:1][C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH2:12])[C:8]=2[Br:13])[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a solution of 2-methyl-6-aminoquinoxaline (15.8 g) in acetic acid (150 mL) was added dropwise a solution of bromine (15.88 g) in acetic acid (11 mL) at 0° C. After the addition, the reaction solution was stirred at 0° C. for one hour, and the precipitates were collected by filtration, washed with ether, and dried to give 2-methyl-6-amino-5-bromoquinoxaline hydrobromide (29.86 g, 94%), which was neutralized to give 2-methyl-6-amino-5-bromoquinoxaline.
Workup
- additionAfter the addition
- filtrationthe precipitates were collected by filtration
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-a296f89623b748929b86ef756e4ab513
- Source dataset
- uspto-grants-2004_07
- Patent number
- US06759429B2
Reaction notes
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