6-Bromo-1-chloro-isoquinoline → 7-Bromo-1-Chloroisoquinoline
Reaction equation
Cl.[Br:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][N+:9]([O-])=[CH:10]2)=[CH:5][CH:4]=1.BrC1C=C2C(=CC=1)C([Cl:25])=NC=C2>>[Br:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][N:9]=[C:10]2[Cl:25])=[CH:5][CH:4]=1Participants
3
Procedure
Compound 37b was prepared from 37a using the procedure described for 1b. 1H-NMR 200 MHz (CDCl3)δ: 7.57-7.88 (3H, m), 8.32 (1H, d, J=6 Hz), 8.51-8.54 (1H, m)
Sources & evidence
- ORD record
- ord-7a7972c47feb4852a4e6e22516446684
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06444672B1
Reaction notes
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