7-Bromo-1-Chloroisoquinoline → 7-Bromo-1-phenoxyisoquinoline
Reaction equation
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][N:8]=[C:9]2Cl)=[CH:4][CH:3]=1.BrC1C=C2C(=CC=1)C([O:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=NC=C2>>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][N:8]=[C:9]2[O:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:4][CH:3]=1Participants
3
Procedure
Compound 37c was prepared from 37b using the procedure described for 1c. 1H-NMR 200 MHz (CDCl3) δ: 6.76-6.97 (2H, m), 7.18-8.09 (7H, m), 8.60-8.64 (1H, m).
Sources & evidence
- ORD record
- ord-4f192a2d7cca422ea53682ee9c5b6538
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06432955B1
Reaction notes
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