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3-Bromoanisole → HCID 16678916, compound

HRID 1661240
Notes
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Reaction equation

HRID 1661240 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:28]=[C:29]([O:33][CH3:34])[CH:30]=[CH:31][CH:32]=1>>[CH3:34][O:33][C:29]1[CH:28]=[C:27]([C:4]([C:6]2[N:7]=[CH:8][N:9]([C:11]3[CH:12]=[C:13]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=4[O:23][CH3:24])[CH:14]=[CH:15][CH:16]=3)[CH:10]=2)=[O:5])[CH:32]=[CH:31][CH:30]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 169713-BromoanisoleHCID 866344291-(2'-Methoxy-biphenyl-3-yl)-1H-imidazole-4-carboxylic acid methoxy-methyl-amide

Product 1

HCID 16678916HCID 16678916, compound

Procedure

This compound is prepared by method C using compound 12c and 3-bromoanisole

Workup

  1. customThis compound is prepared by method C

Sources & evidence

ORD record
ord-a86c69d555e74aef8e9c10ae8ed82a90
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