4-Nitrobenzoyl chloride → HCID 24827156, compound

HRID 2242067Notes

Reaction equation

HRID 2242067 reaction equation
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8](Cl)=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[Cl:13][C:14]1[CH:15]=[N:16][CH:17]=[C:18]([Cl:33])[C:19]=1[CH2:20][C:21]([C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH3:32])[CH:24]=1)=[O:22]>>[Cl:33][C:18]1[CH:17]=[N:16][CH:15]=[C:14]([Cl:13])[C:19]=1/[CH:20]=[C:21](\[O:22][C:8](=[O:9])[C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:12][CH:11]=1)/[C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH3:32])[CH:24]=1

Participants

3

Reactant 2

HCID 85024-Nitrobenzoyl chlorideHCID 668811982-(3,5-Dichloro-pyridin-4-yl)-1-(3,4-dimethoxy-phenyl)-ethanone

Product 1

HCID 24827156HCID 24827156, compound

Procedure

The compound was obtained starting from 4-nitro-benzoyl chloride and 2-(3,5-dichloro-pyridin-4-yl)-1-(3,4-dimethoxy-phenyl)-ethanone, following the procedure of Example 7.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-0e0dfdd5722047eaa99d9f1c74696fbb
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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