4-Methyl-1,2,3,4-tetrahydroisoquinoline → (2-Isopropoxy-5-methanesulfonyl-phenyl)-(4-methyl-3,4-dihydro-1H-isoquinolin-2-yl)-methanone
Reaction equation
[CH3:1][CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][NH:4][CH2:3]1.[CH:12]([O:15][C:16]1[CH:24]=[CH:23][C:22]([S:25]([CH3:28])(=[O:27])=[O:26])=[CH:21][C:17]=1[C:18](O)=[O:19])([CH3:14])[CH3:13]>>[CH:12]([O:15][C:16]1[CH:24]=[CH:23][C:22]([S:25]([CH3:28])(=[O:27])=[O:26])=[CH:21][C:17]=1[C:18]([N:4]1[CH2:3][CH:2]([CH3:1])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5]1)=[O:19])([CH3:14])[CH3:13]Participants
3
Procedure
Prepared in analogy to example 1.1 from 4-methyl-1,2,3,4-tetrahydro-isoquinoline (CA [110841-71-9]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).
Sources & evidence
- ORD record
- ord-4da1c864d4a54a8a8127c026cf985e64
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07442710B2
Reaction notes
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