1-(6-Chlorohexyl)-1H-indole → N-(4-{1-[6-(1H-Indol-1-YL)hexyl]-4-piperidinyl}phenyl)propanamide

HRID 1832979Notes

Reaction equation

HRID 1832979 reaction equation
Cl[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9]1.[NH:17]1[CH2:22][CH2:21][CH:20]([C:23]2[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:33])[CH2:31][CH3:32])=[CH:25][CH:24]=2)[CH2:19][CH2:18]1>>[N:8]1([CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][N:17]2[CH2:22][CH2:21][CH:20]([C:23]3[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:33])[CH2:31][CH3:32])=[CH:25][CH:24]=3)[CH2:19][CH2:18]2)[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9]1

Participants

3

Procedure

Prepared by Procedure AH and Scheme P using 1-(6-chlorohexyl)-1H-indole and N-[4-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 432.3 (M+H)+.

Workup

  1. customPrepared by Procedure AH and Scheme P

Sources & evidence

ORD record
ord-b579199bfa014c90b501919915207eac
Source dataset
uspto-grants-2006_06
Patent number
US07067534B1

Reaction notes

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