Reaction equation
[CH2:1]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][CH:9]=[CH:8]2)[CH3:2].[Cl-].[CH3:13][C:14]1[CH:23]=[CH:22][CH:21]=[CH:20][C:15]=1[CH:16]=[N+:17]([CH3:19])[CH3:18].CC1C=CC=CC=1C=O.CNC>>[CH2:1]([C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[NH:10][CH:9]=[C:8]2[CH:16]([N:17]([CH3:18])[CH3:19])[C:15]1[CH:20]=[CH:21][CH:22]=[CH:23][C:14]=1[CH3:13])[CH3:2]Participants
5
Procedure
The preparation was carried out in accordance with general synthesis instructions 4 from 7-ethyl-1H-indole and (2-methyl-benzylidene)-dimethylammonium chloride, which had been prepared in accordance with example 44 from 2-methyl-benzaldehyde and dimethylamine.
Sources & evidence
- ORD record
- ord-867d92e2aac34594979eadeda21ac344
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07091220B2
Linked notes
Loading…