Reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([N:11]([CH2:19][C:20](O)=[O:21])[C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)(=[O:10])=[O:9])=[N:6][CH:7]=1.[CH2:23]([NH:25][CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)[CH3:24]>>[CH2:23]([N:25]([CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)[C:20](=[O:21])[CH2:19][N:11]([S:8]([C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][N:6]=1)(=[O:10])=[O:9])[C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)[CH3:24]Participants
3
Procedure
prepared by reaction of [(5-methyl-pyridine-2-sulfonyl)-p-tolyl-amino]-acetic acid with ethyl-pyridin-3-ylmethyl-amine
Sources & evidence
- ORD record
- ord-35edc175730542fa955f0ee3d0d5ac9c
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Linked notes
Loading…