4-Phenylpiperidin-4-ol → HCID 19867780, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:17][C:18]([OH:20])=O)[C:5]2[C:6]([CH:16]=1)=[C:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[O:8][N:9]=2.[OH:21][C:22]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:17][C:18]([N:25]2[CH2:26][CH2:27][C:22]([OH:21])([C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[CH2:23][CH2:24]2)=[O:20])[C:5]2[C:6]([CH:16]=1)=[C:7]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[O:8][N:9]=2Participants
3
Procedure
The title compound is prepared by reacting the acid chloride of 5-chloro-3-phenyl-2,1-benzisoxazole-7-acetic acid with 4-hydroxy-4-phenyl-piperidine in an aprotic solvent and washing the reaction mixture with sodium bicarbonate solution.
Workup
- washwashing the reaction mixture with sodium bicarbonate solution
Sources & evidence
- ORD record
- ord-66ec9cde5da74225871a2009e9c7c84b
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04898874
Reaction notes
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