2-Bromoacetamide → HCID 67107643, compound
Reaction equation
[C:1]1([S:7]([CH2:10][C:11]2[C:16]([C:17]([O-:19])=[O:18])=[C:15]([OH:20])[C:14]([C:21]3[CH:25]=[CH:24][O:23][CH:22]=3)=[CH:13][CH:12]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:27][C:28]([NH2:30])=[O:29]>>[C:1]1([S:7]([CH2:10][C:11]2[C:16]([C:17]([O:19][C:11]([CH3:16])([CH3:12])[CH3:10])=[O:18])=[C:15]([O:20][CH2:27][C:28](=[O:29])[NH2:30])[C:14]([C:21]3[CH:25]=[CH:24][O:23][CH:22]=3)=[CH:13][CH:12]=2)(=[O:9])=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
6-(benzenesulphonylmethyl)-3-(furan-3-yl)-2-hydroxybenzoate (Intermediate 120) and 2-bromoacetamide.
Sources & evidence
- ORD record
- ord-e36ba929672c43978e7baa3bfa66b882
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
Loading…