Sodium Hydroxide → (3R,4R)-3-methylpiperidin-4-yl pivalate
Reaction equation
[CH3:1][C@@H:2]1[C@@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1.[OH-].[Na+]>>[CH3:1][C@H:2]1[C@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1Participants
3
Procedure
The mother liquor of 17 from above is treated with 1N—NaOH to obtain the free base which is then crystallized with D-(+)-O,O′-Dibenzoyl tartaric acid as described above to give the antipode 20.
Workup
- customto obtain the free base which
- customis then crystallized with D-(+)-O,O′-Dibenzoyl tartaric acid
- customto give the antipode 20
Sources & evidence
- ORD record
- ord-857af50727a54a0888e06582c994aa87
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858781B2
Reaction notes
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