HCID 422797, compound → HCID 58978315, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([CH2:24][C:25](O)=[O:26])[C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N:21]([CH3:23])[CH3:22])[CH:16]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[N:28]1[C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=[CH:30][C:29]=1[CH2:38][NH:39][CH2:40][CH2:41][OH:42]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([N:21]([CH3:22])[CH3:23])[CH:16]=2)[CH2:24][C:25]([N:39]([CH2:40][CH2:41][OH:42])[CH2:38][C:29]2[CH:30]=[CH:31][C:32]3[C:37](=[CH:36][CH:35]=[CH:34][CH:33]=3)[N:28]=2)=[O:26])(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:2])([CH3:4])[CH3:3]Participants
3
Procedure
prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-(3-dimethylamino-phenyl)-amino]-acetic acid with 2-[(quinolin-2-ylmethyl)-amino]-ethanol
Sources & evidence
- ORD record
- ord-1c8322e8916944e3a8eecd573a38f59d
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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