3-Pyridinylboronic acid → {3-[2-(2-Oxo-oxazolidin-3-ylmethyl)-4-pyridin-3-yl-phenoxy]-phenyl}-acetic acid methyl ester
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]=1Participants
3
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
- customPrepared
Sources & evidence
- ORD record
- ord-19313203e68b43a8ba11a529938b637b
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08242145B2
Reaction notes
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