4-(Piperidin-1-ylmethyl)aniline → HCID 178424133, 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][C:14]=3[CH3:19])[CH:11]=2)[C:6](=[C:20](OCC)[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:5]1=[O:30])(=O)C.[N:31]1([CH2:37][C:38]2[CH:44]=[CH:43][C:41]([NH2:42])=[CH:40][CH:39]=2)[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]1>>[N:31]1([CH2:37][C:38]2[CH:39]=[CH:40][C:41]([NH:42]/[C:20](=[C:6]3\[C:5](=[O:30])[NH:4][C:12]4[C:7]\3=[CH:8][CH:9]=[C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH3:19])[CH:11]=4)/[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)=[CH:43][CH:44]=2)[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36]1Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-6-(2-tolyl)-2-indolinone and 4-(piperidin-1-yl-methyl)-aniline
Sources & evidence
- ORD record
- ord-b683261c87dd49c38b1e334b067685e1
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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