1-Iodo-4-nitrobenzene → 6-Chloro-1-(4-nitrophenyl)-1H-indole
Reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.I[C:12]1[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][N:8]2[C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=2)=[CH:4][CH:3]=1Participants
3
Procedure
Prepared by Procedure C and Scheme O using 6-chloro-1H-indole and 1-iodo-4-nitrobenzene: ESMS m/e: 272.6 (M+H)+.
Workup
- customPrepared by Procedure C and Scheme O
Sources & evidence
- ORD record
- ord-79c9900d0ddf4d2b9878d42c53fc6170
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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