1-(5-Chloropentyl)-1H-indole → N-(4-{1-[5-(1H-Indol-1-YL)pentyl]-4-piperidinyl}phenyl)butanamide
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8]1.[NH:16]1[CH2:21][CH2:20][CH:19]([C:22]2[CH:27]=[CH:26][C:25]([NH:28][C:29](=[O:33])[CH2:30][CH2:31][CH3:32])=[CH:24][CH:23]=2)[CH2:18][CH2:17]1>>[N:7]1([CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:16]2[CH2:21][CH2:20][CH:19]([C:22]3[CH:27]=[CH:26][C:25]([NH:28][C:29](=[O:33])[CH2:30][CH2:31][CH3:32])=[CH:24][CH:23]=3)[CH2:18][CH2:17]2)[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8]1Participants
3
Procedure
Prepared by Procedure AH and Scheme P using 1-(5-chloropentyl)-1H-indole and N-[4-(4-piperidinyl)phenyl]butanamide: ESMS m/e: 432.3 (M+H)+.
Workup
- customPrepared by Procedure AH and Scheme P
Sources & evidence
- ORD record
- ord-54f593157cd04455aef83b375d2f694d
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07067534B1
Reaction notes
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