4-Pyridinepropanol → 2-Methyl-N-(3-{1-[3-(4-pyridinyl)propyl]-4-piperidinyl}phenyl)propanamide
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9]O)=[CH:3][CH:2]=1.[CH3:11][CH:12]([CH3:28])[C:13]([NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([CH:22]2[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[CH:17]=1)=[O:14]>>[CH3:11][CH:12]([CH3:28])[C:13]([NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([CH:22]2[CH2:27][CH2:26][N:25]([CH2:9][CH2:8][CH2:7][C:4]3[CH:3]=[CH:2][N:1]=[CH:6][CH:5]=3)[CH2:24][CH2:23]2)[CH:17]=1)=[O:14]Participants
3
Procedure
Prepared by Procedure O and Scheme W using 3-(4-pyridinyl)-1-propanol and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 366.2 (M+H)+.
Workup
- customPrepared by Procedure O and Scheme W
Sources & evidence
- ORD record
- ord-ce5333ccdfcf4827a0d3e10ef981b580
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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