HCID 19897493, compound → HCID 67894828, compound
Reaction equation
[CH:1]([CH2:3][CH2:4][C:5]12[CH:15]=[CH:14][C:13]([CH3:16])=[C:12]([CH3:17])[CH:6]1[C:7]([NH:9][C:10]2=[O:11])=[O:8])=O.[CH3:18][NH:19][CH2:20][CH2:21][C:22]1[C:31]2[C:26](=[CH:27][C:28]([O:34][CH3:35])=[C:29]([O:32][CH3:33])[CH:30]=2)[CH:25]=[N:24][CH:23]=1>>[CH3:18][N:19]([CH2:20][CH2:21][C:22]1[C:31]2[C:26](=[CH:27][C:28]([O:34][CH3:35])=[C:29]([O:32][CH3:33])[CH:30]=2)[CH:25]=[N:24][CH:23]=1)[CH2:1][CH2:3][CH2:4][C:5]12[CH:15]=[CH:14][C:13]([CH3:16])=[C:12]([CH3:17])[CH:6]1[C:7]([NH:9][C:10]2=[O:11])=[O:8]Participants
3
Procedure
Prepared from 2-(2-formyl-ethyl)-5,6-dimethyl-phthalimide and 4-(2-methylamino-ethyl)-6,7-dimethoxy-isoquinoline analogously to Example 4.
Sources & evidence
- ORD record
- ord-0788480210014c3a902b738b4f7ac18f
- Source dataset
- uspto-grants-1990_03
- Patent number
- US04912115
Reaction notes
Loading…