3-(2-Methoxy-2-oxoethyl)phenylboronic acid, pinacol ester → HCID 66891383, compound

HRID 456205Notes

Reaction equation

HRID 456205 reaction equation
Br[C:2]1[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][C:3]=1[CH2:4][N:5]1[C@@H:9]([CH3:10])[C@@H:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[O:7][C:6]1=[O:17].[CH3:26][O:27][C:28](=[O:45])[CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[C:32](B2OC(C)(C)C(C)(C)O2)[CH:31]=1>>[CH3:26][O:27][C:28](=[O:45])[CH2:29][C:30]1[CH:35]=[C:34]([C:2]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][C:3]=2[CH2:4][N:5]2[C@@H:9]([CH3:10])[C@@H:8]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[O:7][C:6]2=[O:17])[CH:33]=[CH:32][CH:31]=1

Participants

3

Reactant 2

HCID 110977913-(2-Methoxy-2-oxoethyl)phenylboronic acid, pinacol esterHCID 66890163(4S,5R)-3-(2-Bromo-5-trifluoromethyl-benzyl)-4-methyl-5-phenyl-oxazolidin-2-one

Product 1

HCID 66891383HCID 66891383, compound

Procedure

Prepared according to the procedure described in Example 1, Step 4, using the following starting materials: (4S,5R)-3-(2-bromo-5-trifluoromethyl-benzyl)-4-methyl-5-phenyl-oxazolidin-2-one and [3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic acid methyl ester.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-88d2176eedb74c309786c7f55f068641
Source dataset
uspto-grants-2013_07
Patent number
US08497381B2

Reaction notes

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