2-Isopropoxy-5-methylsulfonylbenzoic acid → HCID 58677899, compound
Reaction equation
[CH2:1]([C:3]1([CH2:15][CH3:16])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][NH:5][CH2:4]1)[CH3:2].[CH:17]([O:20][C:21]1[CH:29]=[CH:28][C:27]([S:30]([CH3:33])(=[O:32])=[O:31])=[CH:26][C:22]=1[C:23](O)=[O:24])([CH3:19])[CH3:18]>>[CH2:15]([C:3]1([CH2:1][CH3:2])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=2)[CH2:6][N:5]([C:23]([C:22]2[CH:26]=[C:27]([S:30]([CH3:33])(=[O:32])=[O:31])[CH:28]=[CH:29][C:21]=2[O:20][CH:17]([CH3:19])[CH3:18])=[O:24])[CH2:4]1)[CH3:16]Participants
3
Procedure
Prepared in analogy to example 1.1 from 4,4-diethyl-6-methoxy-1,2,3,4-tetrahydro-isoquinoline and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).
Sources & evidence
- ORD record
- ord-8d330aefb10b41a190b7acc58649523e
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07442710B2
Reaction notes
Loading…