Reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([N:9]([CH2:20][C:21]([OH:23])=O)[S:10]([C:13]2[C:14]([CH3:19])=[CH:15][CH:16]=[CH:17][CH:18]=2)(=[O:12])=[O:11])=[CH:5][CH:4]=1.[CH2:24]([NH:26][CH2:27][C:28]1[N:29]([CH3:33])[CH:30]=[CH:31][CH:32]=1)[CH3:25]>>[CH2:24]([N:26]([CH2:27][C:28]1[N:29]([CH3:33])[CH:30]=[CH:31][CH:32]=1)[C:21](=[O:23])[CH2:20][N:9]([C:6]1[CH:7]=[N:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)[S:10]([C:13]1[C:14]([CH3:19])=[CH:15][CH:16]=[CH:17][CH:18]=1)(=[O:12])=[O:11])[CH3:25]Participants
3
Procedure
prepared by reaction of [(6-methoxy-pyridin-3-yl)-(toluene-2-sulfonyl)-amino]-acetic acid with ethyl-(1-methyl-1H-pyrrol-2-ylmethyl)-amine
Sources & evidence
- ORD record
- ord-15b24145ffa742cf9e2bf8a9055bb2bc
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Linked notes
Loading…