2-(Methylsulfonyl)phenylboronic Acid → {3-[2'-Methanesulfonyl-3-(2-oxo-oxazolidin-3-ylmethyl)-biphenyl-4-yloxy]-4-methoxy-phenyl}-acetic acid ethyl ester

HRID 885384Notes

Reaction equation

HRID 885384 reaction equation
[CH2:1]([O:3][C:4](=[O:29])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18](Br)=[CH:17][C:16]=2[CH2:22][N:23]2[CH2:27][CH2:26][O:25][C:24]2=[O:28])[CH:7]=1)[CH3:2].[CH3:30][S:31]([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1B(O)O)(=[O:33])=[O:32]>>[CH2:1]([O:3][C:4](=[O:29])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([C:35]3[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=3[S:31]([CH3:30])(=[O:33])=[O:32])=[CH:17][C:16]=2[CH2:22][N:23]2[CH2:27][CH2:26][O:25][C:24]2=[O:28])[CH:7]=1)[CH3:2]

Participants

3

Reactant 2

HCID 27735392-(Methylsulfonyl)phenylboronic AcidHCID 58237626{3-[4-Bromo-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester

Product 1

HCID 58237655{3-[2'-Methanesulfonyl-3-(2-oxo-oxazolidin-3-ylmethyl)-biphenyl-4-yloxy]-4-methoxy-phenyl}-acetic acid ethyl ester

Procedure

Prepared according to the procedure described in Example 84, Step 1, using the following starting materials: {3-[4-bromo-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester and 2-methylsulfonylphenylboronic acid.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-30d5b27d8c494bf3b7ef20ce52f9ec2c
Source dataset
uspto-grants-2012_08
Patent number
US08242145B2

Reaction notes

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