1,2,3,4-Tetrahydroisoquinoline-6-carbonitrile → 2-(2-Isopropoxy-5-methanesulfonyl-benzoyl)-1,2,3,4-tetrahydro-isoquinoline-6-carbonitrile
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH2:9][NH:8][CH2:7][CH2:6]2)#[N:2].[CH:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([S:26]([CH3:29])(=[O:28])=[O:27])=[CH:22][C:18]=1[C:19](O)=[O:20])([CH3:15])[CH3:14]>>[CH:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([S:26]([CH3:29])(=[O:28])=[O:27])=[CH:22][C:18]=1[C:19]([N:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][CH:12]=[C:3]([C:1]#[N:2])[CH:4]=2)[CH2:9]1)=[O:20])([CH3:15])[CH3:14]Participants
3
Procedure
Prepared in analogy to example 1.1 from 6-cyano-1,2,3,4-tetrahydro-isoquinoline (CA [166398-34-1]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).
Sources & evidence
- ORD record
- ord-0a819b0767f748f8939487a4a312bbbc
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07442710B2
Reaction notes
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