3-amino-N,N-dimethylbenzylamine → HCID 178486532, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:17](OCC)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:5]1=[O:27])(=O)C.[CH3:28][N:29]([CH2:31][C:32]1[CH:33]=[C:34]([CH:36]=[CH:37][CH:38]=1)[NH2:35])[CH3:30]>>[CH3:30][N:29]([CH2:31][C:32]1[CH:33]=[C:34]([CH:36]=[CH:37][CH:38]=1)[NH:35]/[C:17](=[C:6]1\[C:5](=[O:27])[NH:4][C:12]2[C:7]\1=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)/[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)[CH3:28]Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5,6-dimethoxy-2-indolinone and 3-(dimethylaminomethyl)-aniline
Sources & evidence
- ORD record
- ord-b295b2bbcc364b35bc0f882b8d726651
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
Loading…