4-Acetylbenzoic Acid → 2-(4-Acetylbenzoylamino)-N-(4-methoxyphenyl)benzamide

HRID 395711Notes

Reaction equation

HRID 395711 reaction equation
[NH2:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)=[O:5].[C:19]([C:22]1[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[CH:24][CH:23]=1)(=[O:21])[CH3:20]>>[C:19]([C:22]1[CH:30]=[CH:29][C:25]([C:26]([NH:1][C:2]2[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=2[C:4]([NH:6][C:7]2[CH:8]=[CH:9][C:10]([O:13][CH3:14])=[CH:11][CH:12]=2)=[O:5])=[O:27])=[CH:24][CH:23]=1)(=[O:21])[CH3:20]

Participants

3

Reactant 2

HCID 114704-Acetylbenzoic AcidHCID 4788202-amino-N-(4-methoxyphenyl)benzamide

Product 1

HCID 106439802-(4-Acetylbenzoylamino)-N-(4-methoxyphenyl)benzamideYield 37%

Procedure

Using the procedure described in Example 55, Part B, 2-amino-N-(4-methoxyphenyl)benzamide (1.06 g, 4.36 mmol) was reacted with 4-acetylbenzoic acid to yield 292 mg (37%) of the title compound as a light yellow solid.

Sources & evidence

ORD record
ord-9d461f8ee3884b83a2e113542cf91ceb
Source dataset
uspto-grants-2003_08
Patent number
US06605626B2

Reaction notes

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