2-Bromo-4-methylpyridine → (1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-imidazol-4-yl)-(4-methyl-pyridin-2-yl)-methanone
Reaction equation
CON(C)[C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([C:17]3[C:18]([O:25][CH3:26])=[N:19][C:20]([O:23][CH3:24])=[N:21][CH:22]=3)[CH:12]=2)[CH:10]=1)=[O:5].Br[C:29]1[CH:34]=[C:33]([CH3:35])[CH:32]=[CH:31][N:30]=1>>[CH3:24][O:23][C:20]1[N:19]=[C:18]([O:25][CH3:26])[C:17]([C:13]2[CH:12]=[C:11]([N:9]3[CH:10]=[C:6]([C:4]([C:29]4[CH:34]=[C:33]([CH3:35])[CH:32]=[CH:31][N:30]=4)=[O:5])[N:7]=[CH:8]3)[CH:16]=[CH:15][CH:14]=2)=[CH:22][N:21]=1Participants
3
Procedure
This compound is prepared by method C using compound 12m and 2-bromo-4-methylpyridine
Workup
- customThis compound is prepared by method C
Sources & evidence
- ORD record
- ord-cced342c1ca94d96b1aa0a4705314ce0
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030339B2
Reaction notes
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