Reaction equation
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[Cl-].[CH3:12][C:13]1[CH:25]=[CH:24][CH:23]=[CH:22][C:14]=1[CH:15]=[N+:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([CH:15]([N:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1)[C:14]1[CH:22]=[CH:23][CH:24]=[CH:25][C:13]=1[CH3:12])=[CH:5][NH:6]2Participants
3
Procedure
The preparation was carried out in accordance with general synthesis instructions 4 from 4-methyl-1H-indole and 1-(2-methyl-benzylidene)-piperidinium chloride, which had been prepared in accordance with example 30.
Workup
- customhad been prepared in accordance with example 30
Sources & evidence
- ORD record
- ord-196c1c862b4c4bf289afa7d0c7189a58
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07091220B2
Linked notes
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