2-(4-Chlorophenyl)-1H-indole → {[2-(4-Chlorophenyl)-1H-indol-3-yl]-phenylmethyl}-dimethylamine

HRID 8990

Reaction equation

HRID 8990 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:9][C:10]3[C:15]([CH:16]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:4][CH:3]=1.[Cl-].[CH:18](=[N+:25]([CH3:27])[CH3:26])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:18]([N:25]([CH3:27])[CH3:26])[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 2204632-(4-Chlorophenyl)-1H-indoleHCID 11073839Methanaminium, N-methyl-N-(phenylmethylene)-, chloride

Product 1

HCID 10292040{[2-(4-Chlorophenyl)-1H-indol-3-yl]-phenylmethyl}-dimethylamine

Procedure

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

Workup

  1. customhad been prepared in accordance with example 1

Sources & evidence

ORD record
ord-3e9f91744aff4bafad71878515c662bd
Source dataset
uspto-grants-2006_08
Patent number
US07091220B2

Linked notes

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