Dimethylamine → [(1-Ethyl-2-phenyl-1H-indol-3-yl)-(3-phenoxy-phenyl)-methyl]-dimethylamine

HRID 9074

Reaction equation

[CH2:1]([N:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH3:2].[Cl-].[O:19]([C:26]1[CH:27]=[C:28]([CH:33]=[CH:34][CH:35]=1)[CH:29]=[N+:30]([CH3:32])[CH3:31])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.O(C1C=C(C=CC=1)C=O)C1C=CC=CC=1.CNC>>[CH2:1]([N:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH:29]([N:30]([CH3:32])[CH3:31])[C:28]2[CH:33]=[CH:34][CH:35]=[C:26]([O:19][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:27]=2)=[C:4]1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH3:2]

Participants

Reactant 4

HCID 674Dimethylamine

HCID 382843-Phenoxybenzaldehyde

HCID 832481-ethyl-2-phenyl-1H-indole

HCID 21985375(3-Phenoxy-benzylidene)-dimethylammonium chloride

Product 1

HCID 21985374[(1-Ethyl-2-phenyl-1H-indol-3-yl)-(3-phenoxy-phenyl)-methyl]-dimethylamine

Procedure

The preparation was carried out in accordance with general synthesis instructions 4 from 1-ethyl-2-phenyl-1H-indole and (3-phenoxy-benzylidene)-dimethylammonium chloride, which had been prepared in accordance with example 44 from 3-phenoxy-benzaldehyde and dimethylamine.

Sources & evidence

ORD record: ord-e97e9aacf01447ff9cb577b2ed4fcc56
Source dataset: uspto-grants-2006_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07091220B2

Linked notes

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