6-Bromoisoquinoline 2-oxide → 6-Bromo-7-chloro-isoquinoline 2-oxide
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N+:7]([O-:12])[CH:6]=[CH:5]2.BrC1C=C2C(=CC=1[Cl:24])C=NC=C2>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:24])[CH:8]=[N+:7]([O-:12])[CH:6]=[CH:5]2Participants
3
Procedure
The title compound was prepared by the method, described for 6-Bromo-isoquinoline 2-oxide (4), starting with 6-Bromo-7-chloro-isoquinoline (9). Rt=1.05 min (Method C). Detected mass: 258.1/260.2 (M+H+).
Sources & evidence
- ORD record
- ord-42fb0fe3978847ae87ebdbef7f0b3d9c
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748614B2
Reaction notes
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