2-Bromo-4-methylpyridine → HCID 16678911, compound

HRID 1661235Notes

Reaction equation

HRID 1661235 reaction equation
CON(C)[C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[O:23][CH3:24])[CH:14]=[CH:15][CH:16]=2)[CH:10]=1)=[O:5].Br[C:27]1[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][N:28]=1>>[CH3:24][O:23][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[C:13]1[CH:14]=[CH:15][CH:16]=[C:11]([N:9]2[CH:10]=[C:6]([C:4]([C:27]3[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][N:28]=3)=[O:5])[N:7]=[CH:8]2)[CH:12]=1

Participants

3

Reactant 2

HCID 27340872-Bromo-4-methylpyridineHCID 866344291-(2'-Methoxy-biphenyl-3-yl)-1H-imidazole-4-carboxylic acid methoxy-methyl-amide

Product 1

HCID 16678911HCID 16678911, compound

Procedure

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

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-6ce2953d4aa24a93963fd18c7bfc1f03
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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