4-[2-(3,6-dihydro-2H-pyridin-1-yl)-ethyl]-aniline → HCID 178517253, compound
Reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=2)[NH:13][C:12]1=[O:23])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[N:24]1([CH2:30][CH2:31][C:32]2[CH:38]=[CH:37][C:35]([NH2:36])=[CH:34][CH:33]=2)[CH2:29][CH:28]=[CH:27][CH2:26][CH2:25]1>>[N:24]1([CH2:30][CH2:31][C:32]2[CH:33]=[CH:34][C:35]([NH:36]/[C:4](=[C:11]3\[C:12](=[O:23])[NH:13][C:14]4[C:19]\3=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][CH:15]=4)/[C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=3)=[CH:37][CH:38]=2)[CH2:25][CH:26]=[CH:27][CH2:28][CH2:29]1Participants
3
Procedure
Prepared analogously to Example 89 by reacting 3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone and 4-[2-(3,6-dihydro-2H-pyridin-1-yl)-ethyl]-aniline.
Workup
- customPrepared analogously to Example 89
Sources & evidence
- ORD record
- ord-9a4949d72c9c4ba3965ba1fa55a5fc1a
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
Loading…