m-Anisoyl chloride → HCID 178490483, compound

HRID 1831064Notes

Reaction equation

HRID 1831064 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6](Cl)=[O:7].ClC1C=CC(C([NH:19][C:20]2[CH:21]=[N:22][C:23]([OH:26])=[CH:24][CH:25]=2)=O)=CC=1>>[OH:26][C:23]1[N:22]=[CH:21][C:20]([NH:19][C:6](=[O:7])[C:5]2[CH:9]=[CH:10][CH:11]=[C:3]([O:2][CH3:1])[CH:4]=2)=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 178522254HCID 178522254, compound

Product 1

HCID 178490483HCID 178490483, compound

Procedure

Starting from 3-methoxybenzoyl chloride (1.71 g, 10.0 mmol) and using the procedure as described for the preparation of 4-Chloro-N-(6-hydroxy-pyridin-3-yl)-benzamide yielded the title compound, which was used without further purification.

Sources & evidence

ORD record
ord-e7c21ec4ebbe43679ecd94f6adafceb1
Source dataset
uspto-grants-2006_06
Patent number
US07067517B2

Reaction notes

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