2-Phenylindole → 3-[(2-Chlorophenyl)-piperidin-1-yl-methyl]-2-phenyl-1H-indole

HRID 9011

Reaction equation

HRID 9011 reaction equation
[C:1]1([C:7]2[NH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl-].[Cl:17][C:18]1[CH:30]=[CH:29][CH:28]=[CH:27][C:19]=1[CH:20]=[N+:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1>>[Cl:17][C:18]1[CH:30]=[CH:29][CH:28]=[CH:27][C:19]=1[CH:20]([N:21]1[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]1)[C:15]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8][C:7]=1[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 136982-PhenylindoleHCID 179587471-(2-Chloro-benzylidene)-piperidinium chloride

Product 1

HCID 102723573-[(2-Chlorophenyl)-piperidin-1-yl-methyl]-2-phenyl-1H-indole

Procedure

The preparation was carried out in accordance with general synthesis instructions 4 from 2-phenyl-1H-indole and 1-(2-chloro-benzylidene)-piperidinium chloride, which had been prepared in accordance with example 26.

Workup

  1. customhad been prepared in accordance with example 26

Sources & evidence

ORD record
ord-e753da79418a45e58eb565e7c3d4e2a9
Source dataset
uspto-grants-2006_08
Patent number
US07091220B2

Linked notes

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