Reaction equation
[CH2:1]([N:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH3:2].[Cl-].[CH3:19][C:20]1[CH:31]=[CH:30][CH:29]=[CH:28][C:21]=1[CH:22]=[N+:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1>>[CH2:1]([N:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH:22]([N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)[C:21]2[CH:28]=[CH:29][CH:30]=[CH:31][C:20]=2[CH3:19])=[C:4]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH3:2]Participants
3
Procedure
The preparation was carried out in accordance with general synthesis instructions 4 from 1-ethyl-2-phenyl-1H-indole and 1-(2-methyl-benzylidene)-pyrrolidinium chloride
Sources & evidence
- ORD record
- ord-51710e2fadba4c6ebef8fb7d62ebc731
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07091220B2
Linked notes
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