N-Ethylbenzylamine → HCID 58978396, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([N:8]([CH2:22][C:23]([OH:25])=O)[S:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:14][CH:13]=2)(=[O:11])=[O:10])=[CH:4][CH:3]=1.[CH2:26]([NH:33][CH2:34][CH3:35])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([N:8]([S:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:14][CH:13]=2)(=[O:11])=[O:10])[CH2:22][C:23]([N:33]([CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH2:34][CH3:35])=[O:25])=[CH:4][CH:3]=1Participants
3
Procedure
prepared by reaction of [(6-amino-pyridin-3-yl)-(4-tert-butyl-benzenesulfonyl)-amino]-acetic acid with benzyl-ethyl-amine
Sources & evidence
- ORD record
- ord-282ce286bdbe439aa21c7142c540295a
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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