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3-Pyridinylboronic acid → {3-[2-(2-Oxo-oxazolidin-3-ylmethyl)-4-pyridin-3-yl-phenoxy]-phenyl}-acetic acid methyl ester

HRID 885254
Notes
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Reaction equation

HRID 885254 reaction equation
[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[CH:16][C:15](Br)=[CH:14][C:13]=2[CH2:19][N:20]2[CH2:24][CH2:23][O:22][C:21]2=[O:25])[CH:6]=1.[N:27]1[CH:32]=[CH:31][CH:30]=[C:29](B(O)O)[CH:28]=1>>[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:29]3[CH:28]=[N:27][CH:32]=[CH:31][CH:30]=3)=[CH:14][C:13]=2[CH2:19][N:20]2[CH2:24][CH2:23][O:22][C:21]2=[O:25])[CH:6]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 27343783-Pyridinylboronic acidHCID 58237622{3-[4-Bromo-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-phenyl}-acetic acid methyl ester

Product 1

HCID 58237527{3-[2-(2-Oxo-oxazolidin-3-ylmethyl)-4-pyridin-3-yl-phenoxy]-phenyl}-acetic acid methyl ester

Procedure

Prepared according to the procedure described in Example 7, Step 1, using the following starting materials: {3-[4-bromo-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-phenyl}-acetic acid methyl ester and 3-pyridineboronic acid.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-19313203e68b43a8ba11a529938b637b
Source dataset
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08242145B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes