Sodium Carbonate → [5-(4-Fluoro-3-trifluoromethyl-phenyl)-3-methyl-pyridin-2-yl]-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone
Reaction equation
COC(C1C(C)=CC(C2C=CC=C(C(F)(F)F)C=2)=CN=1)=O.ClC1C=C([C:30]2[CH:31]=[C:32]([CH3:49])[C:33]([C:36]([N:38]3[CH2:43][CH2:42][CH:41]([N:44]4[CH2:48][CH2:47][CH2:46][CH2:45]4)[CH2:40][CH2:39]3)=[O:37])=[N:34][CH:35]=2)C=CC=1Cl.[F:50][C:51]1[CH:56]=[CH:55][C:54](B(O)O)=[CH:53][C:52]=1[C:60]([F:63])([F:62])[F:61].C(=O)([O-])[O-].[Na+].[Na+]>O1CCOCC1.O.[Pd](Cl)Cl>[F:50][C:51]1[CH:56]=[CH:55][C:54]([C:30]2[CH:31]=[C:32]([CH3:49])[C:33]([C:36]([N:38]3[CH2:39][CH2:40][CH:41]([N:44]4[CH2:48][CH2:47][CH2:46][CH2:45]4)[CH2:42][CH2:43]3)=[O:37])=[N:34][CH:35]=2)=[CH:53][C:52]=1[C:60]([F:63])([F:62])[F:61]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
In analogy to the procedure described for the preparation of intermediate 1A, (5-bromo-3-methyl-pyridin-2-yl)-(4-pyrrolidin-1-yl-piperidin-1-yl)-methanone (see example 28) was reacted with 4-fluoro-3-trifluoromethyl-phenyl-boronic acid, (1,1′-bis-diphenylphosphino)-ferrocene)palladium-(II)dichloride (1:1 complex with CH2Cl2) and sodium carbonate in dioxane/water to give the title compound as brown amorphous solid. MS: 436.4 (MH+).
Sources & evidence
- ORD record
- ord-e2b1f237bd6a42ee951eadb4e175be8b
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08227613B2
Reaction notes
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