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2-Bromo-4-methylpyridine → (1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-imidazol-4-yl)-(4-methyl-pyridin-2-yl)-methanone

HRID 1661345
Notes
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Reaction equation

HRID 1661345 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]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 866344351-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-imidazole-4-carboxylic acid methoxy-methyl-amide

Product 1

HCID 16678202(1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-imidazol-4-yl)-(4-methyl-pyridin-2-yl)-methanone

Procedure

This compound is prepared by method C using compound 12m and 2-bromo-4-methylpyridine

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-cced342c1ca94d96b1aa0a4705314ce0
Source dataset
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08030339B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes