Methyl iodide → 1-(2-Methoxy-1,1-dimethyl-ethyl)-4-nitro-1H-imidazole
Reaction equation
[CH3:1][O:2][C:3](=O)[C:4]([CH3:14])([N:6]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[N:8]=[CH:7]1)[CH3:5].[BH4-].[Na+].CI.[H-].[Na+]>CO>[CH3:1][O:2][CH2:3][C:4]([N:6]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[N:8]=[CH:7]1)([CH3:14])[CH3:5]Participants
6
Procedure
2-Methyl-2-(4-nitro-imidazol-1-yl)-propionic acid methyl ester was reduced using sodium borohydride in methanol and the resultant alcohol was alkylated with methyl iodide using sodium hydride as base to provide the title compound: H1 NMR (400 MHz, CDCl3) 1.53 (s, 6H), 3.25 (s, 3H), 3.38 (s, 2H), 7.53 (s, 1H), 7.88 (s, 1H).
Sources & evidence
- ORD record
- ord-f626a9e573d14054950bd48ea89b6e29
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795447B2
Reaction notes
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