2-(Trifluoromethyl)benzeneboronic acid → 5-Bromo-2-(2-(trifluoromethyl)phenyl)pyrimidine
Reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5](I)=[N:6][CH:7]=1.[F:9][C:10]([F:21])([F:20])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1B(O)O>>[Br:1][C:2]1[CH:3]=[N:4][C:5]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([F:21])([F:20])[F:9])=[N:6][CH:7]=1Participants
3
Procedure
Obtained (52% yield) following the procedure described in Intermediate 21, starting with 5-bromo-2-iodopyrimidine and 2-(trifluoromethyl)phenylboronic acid.
Workup
- customObtained (52% yield)
Sources & evidence
- ORD record
- ord-3b57758fd6614679a9a60fa13dd81082
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08536165B2
Reaction notes
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