3-Pyridinylboronic acid → HCID 68783193, 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].[N:19]1[CH:24]=[CH:23][CH:22]=[C:21](B(O)O)[CH:20]=1>>[CH2:1]([O:3][C:4](=[O:18])[CH:5]=[CH:6][C:7]1[C:8]([C:21]2[CH:20]=[N:19][CH:24]=[CH:23][CH:22]=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 (103 mg, 0.368 mmol) was reacted with 3-pyridine boronic acid (2 eq) to give 3-(2-pyridin-3-yl-6-trifluoromethyl-pyridin-3-yl)-acrylic acid ethyl ester (60 mg, 50%).
Sources & evidence
- ORD record
- ord-8789664bccdc4b39821436e599c99029
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858621B2
Reaction notes
Loading…