2-Propoxynaphthalene-1-carbaldehyde → 2-Methyl-N-(3-{1-[(2-propoxy-1-naphthyl)methyl]-4-piperidinyl}phenyl)propanamide
Reaction equation
[CH2:1]([O:4][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]=1[CH:15]=O)[CH2:2][CH3:3].[CH3:17][CH:18]([CH3:34])[C:19]([NH:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([CH:28]2[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]2)[CH:23]=1)=[O:20]>>[CH3:17][CH:18]([CH3:34])[C:19]([NH:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([CH:28]2[CH2:33][CH2:32][N:31]([CH2:15][C:6]3[C:7]4[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=4)[CH:13]=[CH:14][C:5]=3[O:4][CH2:1][CH2:2][CH3:3])[CH2:30][CH2:29]2)[CH:23]=1)=[O:20]Participants
3
Procedure
Prepared by Procedure F and Scheme R using 2-propoxy-1-naphthaldehyde and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 445.2 (M+H)+.
Workup
- customPrepared by Procedure F and Scheme R
Sources & evidence
- ORD record
- ord-0bc47e3974624155837425a57bdf4676
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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