HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121355Generated: November 3, 2026
2-Pyrazinecarboxylic acid → HCID 178513619, compound
https://huagongshe.com/reaction/2121355
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Pyrazinecarboxylic acid | HCID 1047 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2,3-Diaminobenzamide | HCID 10487029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178513619 | HCID 178513619 | 61.9% |
Reaction Steps
A solution of 1.68 g (7.5 mmol) of 2,3-diaminobenzamide and 3.04 g (30 mmol) of triethylamine in 50 ml of dimethylformamide was stirred at room temperature for 1 hour. 0.93 g (7.5 mmol) of pyrazine-2-carboxylic acid and 1.01 g (7.5 mmol) of N-hydroxybenzotriazole (HOBt) were added. After stirring at room temp. for 15 minutes, the mixture was cooled to 0° C. 1.44 g (7.5 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide (EDC) were added, and the mixture was stirred at room temp. for 16 hours. The reaction mixture was then concentrated in vacuo. The residue was partitioned between methylene chloride and saturated sodium bicarbonate solution. The aqueous phase was extracted with methylene chloride. The combined organic phases were dried over magnesium sulfate. The residue obtained after concentration in vacuo was taken up in 50 ml of glacial acetic acid and refluxed for 30 minutes. The reaction mixture was concentrated in vacuo, and the residue was stirred in diethyl ether. The precipitate was removed by filtration and dried at 40° C. in vacuo. 1.11 g of brown crystals were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696437B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-5c3308a3cbd3497a9b53c215226b178c |
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| Source note | uspto-grants-2004_02 |
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