4-Fluorophenylacetyl chloride → 4-{4-[3-(Isobutyrylamino)phenyl]-1-piperidinyl}butyl (4-fluorophenyl)acetate
Reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[CH:13]=[C:14]([NH:18][C:19](=[O:23])[CH:20]([CH3:22])[CH3:21])[CH:15]=[CH:16][CH:17]=2)[CH2:8][CH2:7]1.[F:24][C:25]1[CH:30]=[CH:29][C:28]([CH2:31][C:32](Cl)=[O:33])=[CH:27][CH:26]=1>>[F:24][C:25]1[CH:30]=[CH:29][C:28]([CH2:31][C:32]([O:1][CH2:2][CH2:3][CH2:4][CH2:5][N:6]2[CH2:7][CH2:8][CH:9]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([NH:18][C:19](=[O:23])[CH:20]([CH3:21])[CH3:22])[CH:13]=3)[CH2:10][CH2:11]2)=[O:33])=[CH:27][CH:26]=1Participants
3
Procedure
Prepared by Procedure Q1 and Scheme C2 (TEA) using N-{3-[1-(4-hydroxybutyl)-4-piperidinyl]phenyl}-2-methylpropanamide and (4-fluorophenyl)acetyl chloride: ESMS m/e: 455.3 (M+H)+.
Workup
- customPrepared by Procedure Q1 and Scheme C2 (TEA)
Sources & evidence
- ORD record
- ord-a2170f593a2e45db89f4d9cb329ef41a
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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