4-(Piperidin-1-ylmethyl)aniline → HCID 178465799, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:16][CH2:17][CH3:18])=[C:10]([O:13][CH2:14][CH3:15])[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.[N:30]1([CH2:36][C:37]2[CH:43]=[CH:42][C:40]([NH2:41])=[CH:39][CH:38]=2)[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]1>>[N:30]1([CH2:36][C:37]2[CH:38]=[CH:39][C:40]([NH:41]/[C:19](=[C:6]3\[C:5](=[O:29])[NH:4][C:12]4[C:7]\3=[CH:8][C:9]([O:16][CH2:17][CH3:18])=[C:10]([O:13][CH2:14][CH3:15])[CH:11]=4)/[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)=[CH:42][CH:43]=2)[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35]1Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5,6-diethoxy-2-indolinone and 4-(piperidin-1-yl-methyl)-aniline
Sources & evidence
- ORD record
- ord-7bb9a09a9d8c44adb1afb8f3ad3cc88d
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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