Benzaldehyde, 4-(diphenylamino)- → HCID 22049146, compound
Reaction equation
[C:1]1([N:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:8]2[CH:15]=[CH:14][C:11]([CH:12]=O)=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:22][CH:23]([CH3:39])[C:24]([NH:26][C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([CH:33]2[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]2)[CH:28]=1)=[O:25]>>[C:16]1([N:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:8]2[CH:15]=[CH:14][C:11]([CH2:12][N:36]3[CH2:37][CH2:38][CH:33]([C:29]4[CH:28]=[C:27]([NH:26][C:24](=[O:25])[CH:23]([CH3:39])[CH3:22])[CH:32]=[CH:31][CH:30]=4)[CH2:34][CH2:35]3)=[CH:10][CH:9]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
3
Procedure
Prepared by Procedure F and Scheme R using 4-(diphenylamino)benzaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 504.2 (M+H)+.
Workup
- customPrepared by Procedure F and Scheme R
Sources & evidence
- ORD record
- ord-c69382644ade4ee1bb2189b7a99bc0ce
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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