p-Anisoyl chloride → HCID 24827154, compound

HRID 2242071Notes

Reaction equation

HRID 2242071 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.[Cl:12][C:13]1[CH:14]=[N:15][CH:16]=[C:17]([Cl:32])[C:18]=1[CH2:19][C:20]([C:22]1[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[C:24]([O:30][CH3:31])[CH:23]=1)=[O:21]>>[Cl:32][C:17]1[CH:16]=[N:15][CH:14]=[C:13]([Cl:12])[C:18]=1/[CH:19]=[C:20](\[O:21][C:7](=[O:8])[C:6]1[CH:10]=[CH:11][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)/[C:22]1[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[C:24]([O:30][CH3:31])[CH:23]=1

Participants

3

Reactant 2

HCID 7477p-Anisoyl chlorideHCID 668811982-(3,5-Dichloro-pyridin-4-yl)-1-(3,4-dimethoxy-phenyl)-ethanone

Product 1

HCID 24827154HCID 24827154, compound

Procedure

The compound was obtained starting from 4-methoxy-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-6c2d51bd946f4761b78d9d20208bffdf
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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