1-Ethynyl-3-methoxybenzene → 4-[4-(3-Methoxy-phenylethynyl)-2,5-dimethyl-imidazol-1-yl]-1H-pyridin-2-one
Reaction equation
I[C:2]1[N:3]=[C:4]([CH3:16])[N:5]([C:8]2[CH:13]=[CH:12][N:11](C)[C:10](=[O:15])[CH:9]=2)[C:6]=1[CH3:7].[C:17]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([O:25][CH3:26])[CH:20]=1)#[CH:18]>>[CH3:26][O:25][C:21]1[CH:20]=[C:19]([C:17]#[C:18][C:2]2[N:3]=[C:4]([CH3:16])[N:5]([C:8]3[CH:13]=[CH:12][NH:11][C:10](=[O:15])[CH:9]=3)[C:6]=2[CH3:7])[CH:24]=[CH:23][CH:22]=1Participants
3
Procedure
The title compound, light brown solid, MS: m/e=320.1 (M+H+), was prepared in accordance with the general method of example 1c from 4-(4-iodo-2,5-dimethyl-imidazol-1-yl)-1-methyl-1H-pyridin-2-one and 1-Ethynyl-3-methoxy-benzene.
Sources & evidence
- ORD record
- ord-82210ceebe59494884470c7433f59c51
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08334287B2
Reaction notes
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