(1,1'-Biphenyl)-4-carboxaldehyde → HCID 10183470, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[C:11]1([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:16]=[CH:15][C:14]([CH:17]=O)=[CH:13][CH:12]=1>>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([CH:17]([C:4]1[C:3]3[C:7](=[CH:8][CH:9]=[CH:10][C:2]=3[Cl:1])[NH:6][CH:5]=1)[C:14]1[CH:15]=[CH:16][C:11]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[CH:12][CH:13]=1)=[CH:5][NH:6]2Participants
3
Procedure
The compound Bis(4-chloroindol-3-yl)-(1,1′-biphenyl-4-yl)methane was prepared following general procedure A, starting from 4-chloro indole and 4-biphenyl carboxaldehyde. LC: Tr 2.79 min, MS: 467 (M+H)+
Workup
- customTr 2.79 min, MS
Sources & evidence
- ORD record
- ord-2a278dfab41c45b483bcf914bc55a33c
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07022730B2
Reaction notes
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