Hydrogen Bromide → HCID 178419736, compound
Reaction equation
[BrH:1].C[O:3][C:4]1[N:9]=[CH:8][C:7]([C:10]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13]3=[N:20][N:21]=[CH:22][N:12]3[N:11]=2)=[CH:6][CH:5]=1>>[BrH:1].[N:20]1[N:21]=[CH:22][N:12]2[N:11]=[C:10]([C:7]3[CH:6]=[CH:5][C:4]([OH:3])=[N:9][CH:8]=3)[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[C:13]=12Participants
3
Procedure
47% hydrobromic acid was added to 141 mg of 6-(6-methoxypyridin-3-yl)-[1,2,4]triazolo[3,4-a]phthalazine, and refluxed for 4 hours. The reaction liquid was concentrated under reduced pressure, and ether was added to the resulting residue. The resulting solid was taken out through filtration to obtain 250 mg of 5-[1,2,4]triazolo[3,4-a]phthalazin-6-ylpyridin-2-ol hydrobromide as a brown solid.
Workup
- temperaturerefluxed for 4 hours
- customThe reaction liquid
- concentrationwas concentrated under reduced pressure, and ether
- additionwas added to the resulting residue
- filtrationThe resulting solid was taken out through filtration
Sources & evidence
- ORD record
- ord-13c05ec6216a4439b73e2baaa87efa77
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645756B2
Reaction notes
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