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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374676Generated: October 25, 2026

1,1'-Carbonyldiimidazole → 5-Acetylthiophene-2-carboxylic acid (2-amino-3-carbamoylphenyl)amide

https://huagongshe.com/reaction/2374676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-Acetylthiophene-2-carboxylic acidHCID 3742727—
Reactant2,3-Diaminobenzamide dihydrochlorideHCID 53422807—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
Product5-Acetylthiophene-2-carboxylic acid (2-amino-3-carbamoylphenyl)amideHCID 6735379591%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 5-acetylthiophene-2-carboxylic acid (1.80 g, 10.55 mmol) in pyridine (12 mL) and N,N-dimethylformamide (12 mL) was added 1,1′-carbonyldiimidazole (1.88 g, 11.60 mmol) and the mixture stirred at 45° C. for 4 hours. 2,3-Diaminobenzamide dihydrochloride (synthesized as described in U.S. Pat. No. 6,737,421, column 11, EXAMPLE 2, step (e), 2.36 g, 10.55 mmol) was added and the mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated and the residue partitioned between ethyl acetate and water. The resulting yellow solid was collected by filtration, washed with water and ethyl acetate and dried to give the title compound (2.91 g, 91%). MS (APCI): 304 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462724B2
Source datasetuspto-grants-2008_12
ORD IDord-31b2580e89654a18b3e3e5c8c85a1fa0
Source noteuspto-grants-2008_12