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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673154Generated: October 25, 2026

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

https://huagongshe.com/reaction/1673154

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 Steps

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 treated with 1,1′-carbonyldiimidazole (1.88 g, 11.60 mmol) at 45° C. for 4 hours. 2,3-Diaminobenzamide dihydrochloride (2.36 g, 10.55 mmol) was added and the mixture stirred at ambient temperature overnight. The mixture was concentrated and the residue stirred in ethyl acetate and water, filtered, and the yellow solid 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 numberUS07999117B2
Source datasetuspto-grants-2011_08
ORD IDord-3da9a8fa6d0c40068b21ddca5cfe52b9
Source noteuspto-grants-2011_08