Iodobenzene → Benzyl 1-phenyl-1H-indol-6-YL ether
Reaction equation
[CH2:1]([O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[CH:14][NH:15]2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.I[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[C:19]1([N:15]2[C:16]3[C:12](=[CH:11][CH:10]=[C:9]([O:8][CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)[CH:17]=3)[CH:13]=[CH:14]2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Participants
3
Procedure
Prepared by Procedure C and Scheme O using 6-(benzyloxy)-1H-indole and iodobenzene: ESMS m/e: 300.0 (M+H)+.
Workup
- customPrepared by Procedure C and Scheme O
Sources & evidence
- ORD record
- ord-9bd9dd0c6d75463293614f4e61864ba9
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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