4-{[Benzyl(methyl)amino]methyl}aniline → HCID 178482716, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH:11]=2)[C:6](=[C:19](OCC)[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:5]1=[O:29])(=O)C.[CH2:30]([N:37]([CH2:39][C:40]1[CH:46]=[CH:45][C:43]([NH2:44])=[CH:42][CH:41]=1)[CH3:38])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>>[CH2:30]([N:37]([CH2:39][C:40]1[CH:41]=[CH:42][C:43]([NH:44]/[C:19](=[C:6]2\[C:5](=[O:29])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:11]=3)/[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)=[CH:45][CH:46]=1)[CH3:38])[C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-6-phenyl-2-indolinone and 4-[(N-benzyl-N-methyl-amino)-methyl]-aniline
Sources & evidence
- ORD record
- ord-43f9c4737c1145f9a05c63ad042a9bc3
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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