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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 5-Acetylthiophene-2-carboxylic acid | HCID 3742727 | — |
| Reactant | 2,3-Diaminobenzamide dihydrochloride | HCID 53422807 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Acetylthiophene-2-carboxylic acid (2-amino-3-carbamoylphenyl)amide | HCID 67353795 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462724B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-31b2580e89654a18b3e3e5c8c85a1fa0 |
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| Source note | uspto-grants-2008_12 |
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