4-{[Benzyl(methyl)amino]methyl}aniline → HCID 178487307, compound

HRID 1007438Notes

Reaction equation

HRID 1007438 reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:15](OCC)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:5]1=[O:25])(=O)C.[CH2:26]([N:33]([CH2:35][C:36]1[CH:42]=[CH:41][C:39]([NH2:40])=[CH:38][CH:37]=1)[CH3:34])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH2:26]([N:33]([CH2:35][C:36]1[CH:37]=[CH:38][C:39]([NH:40]/[C:15](=[C:6]2\[C:5](=[O:25])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=3)/[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:41][CH:42]=1)[CH3:34])[C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1

Participants

3

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-6-methoxy-2-indolinone and 4-[(N-benzyl-N-methyl-amino)-methyl]-aniline

Sources & evidence

ORD record
ord-f195a3a7f94b4adf8ba0269e2419e055
Source dataset
uspto-grants-2004_09
Patent number
US06794395B1

Reaction notes

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