Lithium Hydroxide → HCID 53704113, compound
Reaction equation
[F:1][C:2]([F:29])([F:28])[C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([N:11]3[CH2:16][CH2:15][CH2:14][CH2:13][C@H:12]3[C:17]([O:19]CC3C=CC=CC=3)=[O:18])=[N:8][C:7]=2[CH:27]=1.[OH-].[Li+]>>[F:28][C:2]([F:1])([F:29])[C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([N:11]3[CH2:16][CH2:15][CH2:14][CH2:13][C@H:12]3[C:17]([OH:19])=[O:18])=[N:8][C:7]=2[CH:27]=1Participants
3
Procedure
The title compound was prepared by a similar method to Preparation 3 from benzyl (2S)-1-[5-(trifluoromethyl)-1,3-benzoxazol-2-yl]-2-piperidinecarboxylate [see Preparation 30] and 1N aqueous lithium hydroxide solution to afford (2S)-1-[5-(trifluoromethyl)-1,3-benzoxazol-2-yl]-2-piperidinecarboxylic acid as an oil.
Sources & evidence
- ORD record
- ord-43f0e6d7b42645b8a02497742072ee32
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06686357B1
Reaction notes
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