tert-Butyl bromoacetate → [(5-Isopropyl-pyridine-2-sulfonyl)-p-tolyl-amino]-acetic acid
Reaction equation
[C:1]1([CH3:20])[CH:6]=[CH:5][C:4]([NH:7][S:8]([C:11]2[CH:16]=[CH:15][C:14]([CH:17]([CH3:19])[CH3:18])=[CH:13][N:12]=2)(=[O:10])=[O:9])=[CH:3][CH:2]=1.Br[CH2:22][C:23]([O:25]C(C)(C)C)=[O:24]>>[CH:17]([C:14]1[CH:15]=[CH:16][C:11]([S:8]([N:7]([CH2:22][C:23]([OH:25])=[O:24])[C:4]2[CH:3]=[CH:2][C:1]([CH3:20])=[CH:6][CH:5]=2)(=[O:10])=[O:9])=[N:12][CH:13]=1)([CH3:18])[CH3:19]Participants
3
Procedure
prepared by reaction of 5-isopropyl-pyridine-2-sulfonic acid p-tolylamide with tert-butyl bromoacetate
Sources & evidence
- ORD record
- ord-ef6b01aa8c6443faabd35851c62d652e
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435815B2
Reaction notes
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