[(4-tert-Butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid → HCID 58978406, 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][C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([CH2:35][NH:36][CH2:37][CH3:38])[N:30]=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:36]([CH2:37][CH3:38])[CH2:35][C:31]2[CH:32]=[CH:33][CH:34]=[C:29]([NH:28][CH2:26][CH3:27])[N:30]=2)=[O:25])(=[O:12])=[O:13])=[CH:7][CH:6]=1)([CH3:2])([CH3:4])[CH3:3]Participants
3
Procedure
prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid with ethyl-(6-ethylaminomethyl-pyridin-2-yl)-amine
Sources & evidence
- ORD record
- ord-b8ea5d499e1b4933b6d086e2a99a39d2
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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