[(4-tert-Butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid → HCID 10346675, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([CH2:22][C:23]([OH:25])=O)[C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:26]([NH:28][CH2:29][C:30]1[N:35]=[C:34]([N:36]([CH3:38])[CH3:37])[CH:33]=[CH:32][CH:31]=1)[CH3:27]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([C:15]2[CH:16]=[CH:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[CH2:22][C:23]([N:28]([CH2:29][C:30]2[CH:31]=[CH:32][CH:33]=[C:34]([N:36]([CH3:37])[CH3:38])[N:35]=2)[CH2:26][CH3:27])=[O:25])(=[O:12])=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid with (6-ethylaminomethyl-pyridin-2-yl)-dimethyl-amine
Sources & evidence
- ORD record
- ord-8f623f3a3d504587acc4955022e3aa9c
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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