2-Bromo-3-methylpyridine → HCID 67429493, compound

HRID 1661247Notes

Reaction equation

HRID 1661247 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[C:23]#[N:24])[CH:14]=[CH:15][CH:16]=2)[CH:10]=1)=[O:5].Br[C:27]1[C:32]([CH3:33])=[CH:31][CH:30]=[CH:29][N:28]=1>>[CH3:33][C:32]1[C:27]([C:4]([C:6]2[N:7]=[CH:8][N:9]([C:11]3[CH:12]=[C:13]([C:17]4[C:18]([C:23]#[N:24])=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH:14]=[CH:15][CH:16]=3)[CH:10]=2)=[O:5])=[N:28][CH:29]=[CH:30][CH:31]=1

Participants

3

Reactant 2

HCID 2208322-Bromo-3-methylpyridineHCID 866344301-(2'-Cyano-biphenyl-3-yl)-1H-imidazole-4-carboxylic acid methoxy-methyl-amide

Product 1

HCID 67429493HCID 67429493, compound

Procedure

This compound is prepared by method C using compound 12d and 2-bromo-3-methylpyridine.

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-5f6bd7cebf6a4958abe74d7b538d33a8
Source dataset
uspto-grants-2011_10
Patent number
US08030339B2

Reaction notes

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