3,5-Bis-trifluoromethylphenylboronic acid → (3,5-Dimethyl-3',5'-bis-trifluoromethyl-biphenyl-4-yl)-[4-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanone
Reaction equation
Br[C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([C:9]([N:11]2[CH2:16][CH2:15][CH:14]([N:17]3[CH2:21][CH2:20][CH2:19][C@H:18]3[CH2:22][OH:23])[CH2:13][CH2:12]2)=[O:10])=[C:4]([CH3:24])[CH:3]=1.[F:25][C:26]([F:41])([F:40])[C:27]1[CH:28]=[C:29](B(O)O)[CH:30]=[C:31]([C:33]([F:36])([F:35])[F:34])[CH:32]=1>>[CH3:24][C:4]1[CH:3]=[C:2]([C:29]2[CH:30]=[C:31]([C:33]([F:36])([F:34])[F:35])[CH:32]=[C:27]([C:26]([F:25])([F:41])[F:40])[CH:28]=2)[CH:7]=[C:6]([CH3:8])[C:5]=1[C:9]([N:11]1[CH2:16][CH2:15][CH:14]([N:17]2[CH2:21][CH2:20][CH2:19][C@H:18]2[CH2:22][OH:23])[CH2:13][CH2:12]1)=[O:10]Participants
3
Reactant 2
Product 1
Procedure
In analogy to the procedure described for example 1, (4-bromo-2,6-dimethyl-phenyl)-[4-((S)-2-hydroxymethyl-pyrrolidin-1-yl)-piperidin-1-yl]-methanone (intermediate 4) was reacted with 3,5-bis-trifluoromethyl-phenyl boronic acid to give the title compound as colorless solid. MS: 529.2 (MH+).
Sources & evidence
- ORD record
- ord-15bba9603b1b480d89eadf90444d114c
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08153805B2
Reaction notes
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