P-Anisidine → N-(4-methoxyphenyl)-3-(phenylsulfonyl)benzamide

HRID 1967530Notes

Reaction equation

HRID 1967530 reaction equation
[C:1]1([S:7]([C:10]2[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=2)[C:13]([OH:15])=O)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:19][O:20][C:21]1[CH:27]=[CH:26][C:24]([NH2:25])=[CH:23][CH:22]=1>>[CH3:19][O:20][C:21]1[CH:27]=[CH:26][C:24]([NH:25][C:13](=[O:15])[C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([S:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)(=[O:8])=[O:9])[CH:11]=2)=[CH:23][CH:22]=1

Participants

3

Reactant 2

HCID 7732P-AnisidineHCID 2385993-(Phenylsulfonyl)benzoic acid

Product 1

HCID 66872344N-(4-methoxyphenyl)-3-(phenylsulfonyl)benzamide

Procedure

The entitled compound was produced according to the method of Example 92 but using 3-(phenylsulfonyl)benzoic acid and 4-methoxyaniline as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-39e6a644ff08445b882101610bf14418
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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