Methyl bromoacetate → [(2-Methoxy-phenyl)-(3-methyl-pyridine-2-sulfonyl)-amino]-acetic acid
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[NH:9][S:10]([C:13]1[C:18]([CH3:19])=[CH:17][CH:16]=[CH:15][N:14]=1)(=[O:12])=[O:11].Br[CH2:21][C:22]([O:24]C)=[O:23]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]([CH2:21][C:22]([OH:24])=[O:23])[S:10]([C:13]1[C:18]([CH3:19])=[CH:17][CH:16]=[CH:15][N:14]=1)(=[O:11])=[O:12]Participants
3
Procedure
prepared by reaction of 3-methyl-pyridine-2-sulfonic acid (2-methoxy-phenyl)-amide with methyl bromoacetate
Sources & evidence
- ORD record
- ord-71632ca1c48146a99dd0af9febfc7aff
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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