3-Fluorophenylboronic acid → HCID 68782363, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:18])[CH:5]=[CH:6][C:7]1[C:8](Cl)=[N:9][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:11][CH:12]=1)[CH3:2].[F:19][C:20]1[CH:21]=[C:22](B(O)O)[CH:23]=[CH:24][CH:25]=1>>[CH2:1]([O:3][C:4](=[O:18])[CH:5]=[CH:6][C:7]1[C:8]([C:24]2[CH:23]=[CH:22][CH:21]=[C:20]([F:19])[CH:25]=2)=[N:9][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:11][CH:12]=1)[CH3:2]Participants
3
Procedure
3-(2-Chloro-6-trifluoromethyl-pyridin-3-yl)-acrylic acid ethyl ester (110 mg, 0.393 mmol) was reacted with 3-fluorophenyl boronic acid (2 eq) to give 3-[2-(3-fluoro-phenyl)-6-trifluoromethyl-pyridin-3-yl]-acrylic acid ethyl ester (70 mg, 53%).
Sources & evidence
- ORD record
- ord-da9dcbb9ea5a4a7bbcb9c672777faec1
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858621B2
Reaction notes
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