4-(Piperidin-1-ylmethyl)aniline → HCID 178456757, 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)[CH2:18][CH3:19])[C:5]1=[O:23])(=O)C.[N:24]1([CH2:30][C:31]2[CH:37]=[CH:36][C:34]([NH2:35])=[CH:33][CH:32]=2)[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1>>[N:24]1([CH2:30][C:31]2[CH:32]=[CH:33][C:34]([NH:35]/[C:17](=[C:6]3\[C:5](=[O:23])[NH:4][C:12]4[C:7]\3=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=4)/[CH2:18][CH3:19])=[CH:36][CH:37]=2)[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]1Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-ethyl-methylidene)-5,6-dimethoxy-2-indolinone and 4-(piperidin-1-yl-methyl)-aniline
Sources & evidence
- ORD record
- ord-3d403699ce97432c9d3c2793a68a759d
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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