2,5-Dimethoxybenzoic acid → HCID 18687414, compound
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.[CH3:13][O:14][C:15]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][C:16]=1[C:17](O)=[O:18]>>[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:17](=[O:18])[C:16]2[CH:20]=[C:21]([O:24][CH3:25])[CH:22]=[CH:23][C:15]=2[O:14][CH3:13])[CH2:7]1Participants
3
Procedure
The title compound was prepared in an analogous manner to Example 1 from 5-amino-2-methyl-1,2,3,4-tetrahydroisoquinoline and 2,5-dimethoxybenzoic acid.
Sources & evidence
- ORD record
- ord-e10caef5760145228327a4c3bfd4a4ce
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110934
Reaction notes
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