Hydrogen Bromide → HCID 68898104, compound
Reaction equation
[NH2:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[C:6]([O:15]C)[C:7]([Cl:14])=[CH:8][C:9]=2[Cl:13])[N:4]=[CH:3]1.[BrH:17]>>[BrH:17].[NH2:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[C:6]([OH:15])[C:7]([Cl:14])=[CH:8][C:9]=2[Cl:13])[N:4]=[CH:3]1Participants
3
Procedure
A solution of 5-3 (60 mg, 0.231 mmol) and 48% aqueous hydrobromic acid (2 mL) was heated at 120° C. for 2 h. The solution was cooled to room temperature and the precipitate was isolated via filtration, washed successively with dichloromethane and diethyl ether, and dried in vacuo to provide 3-amino-5,7-dichloro-8-hydroxy-3H-quinazolin-4-one hydrobromide (5-4) as a white solid (44 mg, 58%).
Workup
- customthe precipitate was isolated via filtration
- washwashed successively with dichloromethane and diethyl ether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-0f68f65f3a0948e6b4a2eba7f99c9f5f
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084459B2
Reaction notes
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