Benzaldehyde, 4-(diphenylamino)- → {3-[3-Benzyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}[4-(Diphenylamino)Benzyl]Amine
Reaction equation
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:29]1([N:35]([C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)[C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>>[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:40][C:39]3[CH:38]=[CH:37][C:36]([N:35]([C:44]4[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=4)[C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)=[CH:43][CH:42]=3)[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:26])[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 4-diphenylamino-benzaldehyde. MS (ESI) m/z 636.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-25436e3751494360a8b322284d9cc646
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
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