Methyl iodide → 5-[2-(2,4-Dichloro-phenyl)-propionyl]-1-methyl-1H-pyridin-2-one
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH3:19])[C:10]([C:12]1[CH:13]=[CH:14][C:15](=[O:18])[NH:16][CH:17]=1)=[O:11].I[CH3:21]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH3:19])[C:10]([C:12]1[CH:13]=[CH:14][C:15](=[O:18])[N:16]([CH3:21])[CH:17]=1)=[O:11]Participants
3
Procedure
In analogy to Example 195, 5-[2-(2,4-dichloro-phenyl)-propionyl]-1H-pyridin-2-one was alkylated with iodomethane to give the title compound as a colorless oil. MS (m/e)=310.1 [M+H+].
Sources & evidence
- ORD record
- ord-c4d21e15de894b57b0581a605e258644
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08143280B2
Reaction notes
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