1-(5-Chloropentyl)-1H-indole → N-(4-{1-[5-(1H-Indol-1-YL)pentyl]-4-piperidinyl}phenyl)-2-methylpropanamide
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.[CH3:16][CH:17]([CH3:33])[C:18]([NH:20][C:21]1[CH:26]=[CH:25][C:24]([CH:27]2[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]2)=[CH:23][CH:22]=1)=[O:19]>>[N:7]1([CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:30]2[CH2:31][CH2:32][CH:27]([C:24]3[CH:25]=[CH:26][C:21]([NH:20][C:18](=[O:19])[CH:17]([CH3:16])[CH3:33])=[CH:22][CH:23]=3)[CH2:28][CH2:29]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 2-methyl-N-[4-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 432.3 (M+H)+.
Workup
- customPrepared by Procedure AH and Scheme P
Sources & evidence
- ORD record
- ord-06929982d68042a6a92ff33fa5279cc5
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Reaction notes
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