2-methyl-N-[3-(4-piperidyl)phenyl]propanamide → HCID 69524225, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C@H:9]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:10][CH2:11]Cl)=[CH:4][C:3]=1[Cl:19].[CH3:20][CH:21]([CH3:37])[C:22]([NH:24][C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([CH:31]2[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]2)[CH:26]=1)=[O:23]>>[Cl:19][C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][C:2]=1[Cl:1])[O:8][C@H:9]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:10][CH2:11][N:34]1[CH2:35][CH2:36][CH:31]([C:27]2[CH:26]=[C:25]([NH:24][C:22](=[O:23])[CH:21]([CH3:20])[CH3:37])[CH:30]=[CH:29][CH:28]=2)[CH2:32][CH2:33]1Participants
3
Procedure
Prepared by Procedure A using 1,2-dichloro-4-{[(1S)-3-chloro-1-phenylpropyl]oxy}benzene and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 525.3 (M+H)+.
Sources & evidence
- ORD record
- ord-1be5f3d63f5946e3bbfa50a3424a2420
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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