3-Hydroxyacetophenone → HCID 22049339, compound
Reaction equation
[OH:1][CH:2]([C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[CH:25][CH:24]=1)[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:12]=[C:13]([NH:17][C:18](=[O:22])[CH:19]([CH3:21])[CH3:20])[CH:14]=[CH:15][CH:16]=2)[CH2:7][CH2:6]1.[C:31]([C:34]1[CH:35]=[C:36](O)[CH:37]=[CH:38][CH:39]=1)(=[O:33])[CH3:32]>>[C:31]([C:34]1[CH:39]=[C:38]([CH:37]=[CH:36][CH:35]=1)[O:1][CH:2]([C:23]1[CH:24]=[CH:25][C:26]([O:29][CH3:30])=[CH:27][CH:28]=1)[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][CH:8]([C:11]2[CH:12]=[C:13]([NH:17][C:18](=[O:22])[CH:19]([CH3:21])[CH3:20])[CH:14]=[CH:15][CH:16]=2)[CH2:7][CH2:6]1)(=[O:33])[CH3:32]Participants
3
Procedure
Prepared by Procedure A and Scheme AN using N-(3-{1-[3-hydroxy-3-(4-methoxyphenyl)propyl]-4-piperidinyl}phenyl)-2-methylpropanamide and 3-acetylphenol: ESMS m/e: 529.0 (M+H)+.
Sources & evidence
- ORD record
- ord-15bf259a176b4f0ba314f9ade26c2c5a
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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