2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-amine → N-(2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-4-n-butyl-2-methoxy-5-chloro-benzamide, Hydrochloride
Reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([CH3:12])[CH2:7]2.[CH2:13]([C:17]1[C:25]([Cl:26])=[CH:24][C:20]([C:21](O)=[O:22])=[C:19]([O:27][CH3:28])[CH:18]=1)[CH2:14][CH2:15][CH3:16]>>[ClH:26].[CH3:12][N:6]1[CH2:5][CH2:4][C:3]2[C:8](=[CH:9][CH:10]=[CH:11][C:2]=2[NH:1][C:21](=[O:22])[C:20]2[CH:24]=[C:25]([Cl:26])[C:17]([CH2:13][CH2:14][CH2:15][CH3:16])=[CH:18][C:19]=2[O:27][CH3:28])[CH2:7]1Participants
3
Procedure
The title compound was prepared in a similar manner to Example 1 from 5-amino-2-methyl-1,2,3,4-tetrahydroisoquinoline and 4-n-butyl-2-methoxy-5-chlorobenzoic acid.
Sources & evidence
- ORD record
- ord-e9de278d754b488c9cf5f7beaf3133d8
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110934
Reaction notes
Loading…