4-(3-Chloropropyl)pyridine → HCID 23177330, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][CH2:9][N:10]2[CH2:19][CH2:18][C:17]3[C:12](=[CH:13][C:14]([O:22][CH3:23])=[C:15]([O:20][CH3:21])[CH:16]=3)[C:11]2=[O:24])[CH:2]=1.[Cl:25][CH2:26][CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=1>>[OH2:20].[OH2:20].[ClH:25].[ClH:25].[N:32]1[CH:33]=[CH:34][C:29]([CH2:28][CH2:27][CH2:26][N:1]2[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][CH2:8][CH2:9][N:10]3[CH2:19][CH2:18][C:17]4[C:12](=[CH:13][C:14]([O:22][CH3:23])=[C:15]([O:20][CH3:21])[CH:16]=4)[C:11]3=[O:24])[CH2:2]2)=[CH:30][CH:31]=1Participants
3
Procedure
Prepared from 2-[3-(pyrid-3-yl)-propyl]-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 4-(3-chloropropyl)-pyridine analogously to Example 1.
Sources & evidence
- ORD record
- ord-27be51b74e8644ee8c87d7bfc5168b88
- Source dataset
- uspto-grants-1992_12
- Patent number
- US05175157
Reaction notes
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