Dimethyl Sulfate → HCID 21936532, compound
Reaction equation
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:12])[CH:8]=2)[N:3]=1.[CH3:13][O:14][S:15]([O:18]C)(=[O:17])=[O:16]>>[CH3:13][O:14][S:15]([O-:18])(=[O:17])=[O:16].[CH3:13][N+:3]1[C:4]2[C:9](=[CH:8][C:7]([CH3:12])=[CH:6][CH:5]=2)[CH:10]=[CH:11][C:2]=1[CH3:1]Participants
3
Procedure
2,6-Dimethylquinoline (4.78 g, 30 mmol) was alkylated with dimethylsulphate (3.78 g, 30 mmol) as above to give the title compound (7.9 g, 28.5 mmol, 95%).
Sources & evidence
- ORD record
- ord-ec2c2bc367dc4619872a7de70bb03b9e
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115619B2
Reaction notes
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