2-Isopropoxy-5-methylsulfonylbenzoic acid → HCID 58677897, compound
Reaction equation
[CH2:1]([CH:3]1[C:12]2[C:7](=[CH:8][C:9]([O:13][CH3:14])=[CH:10][CH:11]=2)[CH2:6][NH:5][CH2:4]1)[CH3:2].[CH:15]([O:18][C:19]1[CH:27]=[CH:26][C:25]([S:28]([CH3:31])(=[O:30])=[O:29])=[CH:24][C:20]=1[C:21](O)=[O:22])([CH3:17])[CH3:16]>>[CH2:1]([CH:3]1[C:12]2[C:7](=[CH:8][C:9]([O:13][CH3:14])=[CH:10][CH:11]=2)[CH2:6][N:5]([C:21]([C:20]2[CH:24]=[C:25]([S:28]([CH3:31])(=[O:30])=[O:29])[CH:26]=[CH:27][C:19]=2[O:18][CH:15]([CH3:17])[CH3:16])=[O:22])[CH2:4]1)[CH3:2]Participants
3
Procedure
Prepared in analogy to example 1.1 from 4-ethyl-7-methoxy-1,2,3,4-tetrahydro-isoquinoline and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).
Sources & evidence
- ORD record
- ord-fb025bb00f754e678f90a79eb2e2a331
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07442710B2
Reaction notes
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