4-(Piperidin-1-ylmethyl)aniline → HCID 178516980, compound
Reaction equation
CO[C:3](=[C:10]1[C:18]2[C:13](=[CH:14][C:15]3[O:21][CH2:20][O:19][C:16]=3[CH:17]=2)[NH:12][C:11]1=[O:22])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[N:23]1([CH2:29][C:30]2[CH:36]=[CH:35][C:33]([NH2:34])=[CH:32][CH:31]=2)[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1>>[N:23]1([CH2:29][C:30]2[CH:31]=[CH:32][C:33]([NH:34]/[C:3](=[C:10]3\[C:11](=[O:22])[NH:12][C:13]4[C:18]\3=[CH:17][C:16]3[O:19][CH2:20][O:21][C:15]=3[CH:14]=4)/[C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)=[CH:35][CH:36]=2)[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28]1Participants
3
Procedure
Prepared from 3-(1-methoxy-1-phenyl-methylidene)-5,6-methylenedioxy-2-indolinone and 4-(piperidin-1-yl-methyl)-aniline
Sources & evidence
- ORD record
- ord-63a4a8fb2cb942e59e6685bde4f7af0d
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
Loading…