Acetamide → Methyl 3-acetylamino-5-(2-oxopyrrolidin-1-yl)benzoate
Reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][C:13]2=[O:17])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[C:18]([NH2:21])(=[O:20])[CH3:19]>>[C:18]([NH:21][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([N:12]2[CH2:16][CH2:15][CH2:14][C:13]2=[O:17])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6])(=[O:20])[CH3:19]Participants
3
Procedure
D12 was prepared as for E1, from methyl 3-bromo-5-(2-oxopyrrolidin-1-yl)benzoate and acetamide.
Sources & evidence
- ORD record
- ord-d4c23a0151ea4483bdb85d1f3ea2e260
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992103B2
Reaction notes
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