2-(((2S,3R)-1-(5-Fluoro-2-(pyrimidin-2-yl)benzoyl)-3-methylpiperidin-2-yl)methyl)isoindoline-1,3-dione → ((2S,3R)-2-(Aminomethyl)-3-methylpiperidin-1-yl)(5-fluoro-2-(pyrimidin-2-yl)phenyl)methanone
Reaction equation
NC[C@@H]1[C@H](C)CCCN1C(C1C=C(C)C=CC=1C1C=NN(C)C=1)=O.[F:25][C:26]1[CH:27]=[CH:28][C:29]([C:53]2[N:58]=[CH:57][CH:56]=[CH:55][N:54]=2)=[C:30]([CH:52]=1)[C:31]([N:33]1[CH2:38][CH2:37][CH2:36][C@@H:35]([CH3:39])[C@H:34]1[CH2:40][N:41]1C(=O)C2C(=CC=CC=2)C1=O)=[O:32]>>[NH2:41][CH2:40][C@@H:34]1[C@H:35]([CH3:39])[CH2:36][CH2:37][CH2:38][N:33]1[C:31]([C:30]1[CH:52]=[C:26]([F:25])[CH:27]=[CH:28][C:29]=1[C:53]1[N:54]=[CH:55][CH:56]=[CH:57][N:58]=1)=[O:32]Participants
3
Reactant 2
Product 1
Procedure
The title compound was synthesized following the same general protocol as described for ((2S,3R)-2-(aminomethyl)-3-methylpiperidin-1-yl)(5-methyl-2-(1-methyl-1H-pyrazol-4-yl)phenyl)methanone in Example A1, using 2-(((2S,3R)-1-(5-fluoro-2-(pyrimidin-2-yl)benzoyl)-3-methylpiperidin-2-yl)methyl)isoindoline-1,3-dione. ESI-MS (m/z): 329 [M+1]+.
Sources & evidence
- ORD record
- ord-4b143b234a21493cbbcc6cdf4c4159c6
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440982B2
Reaction notes
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