1-(4-Chlorobutyl)-1H-indole → N-(4-{1-[4-(1H-Indol-1-YL)butyl]-4-piperidinyl}phenyl)butanamide
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7]1.[NH:15]1[CH2:20][CH2:19][CH:18]([C:21]2[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:32])[CH2:29][CH2:30][CH3:31])=[CH:23][CH:22]=2)[CH2:17][CH2:16]1>>[N:6]1([CH2:5][CH2:4][CH2:3][CH2:2][N:15]2[CH2:20][CH2:19][CH:18]([C:21]3[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:32])[CH2:29][CH2:30][CH3:31])=[CH:23][CH:22]=3)[CH2:17][CH2:16]2)[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7]1Participants
3
Procedure
Prepared by Procedure AH and Scheme P using 1-(4-chlorobutyl)-1H-indole and N-[4-(4-piperidinyl)phenyl]butanamide: ESMS m/e: 418.2 (M+H)+.
Workup
- customPrepared by Procedure AH and Scheme P
Sources & evidence
- ORD record
- ord-6b5cbb3c227d4118a68c6b4cb78badfd
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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