2-Bromopyridine → {1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-imidazol-4-yl}-pyridin-2-yl-methanone

HRID 1661343Notes

Reaction equation

HRID 1661343 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]=[CH:33][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]=[CH:33][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]=1

Participants

3

Procedure

This compound is prepared by method C using compound 12m and 2-bromopyridine

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-cfdc722de0c54292b067b859857d22ef
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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