HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462301Generated: October 25, 2026
Hydrochloric Acid → 2,3-Dicyano-5-(1-carboxy-n-propyl)amino-6-phenylpyrazine
https://huagongshe.com/reaction/1462301
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Alpha-Aminobutyric Acid | HCID 6657 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Chloro-6-phenylpyrazine-2,3-dicarbonitrile | HCID 12907205 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Dicyano-5-(1-carboxy-n-propyl)amino-6-phenylpyrazine | HCID 13336970 | 86% |
Reaction Steps
2,3-Dicyano-5-chloro-6-phenylpyrazine (2.41 g; 0.01 mole) was dissolved in 30 ml of tetrahydrofuran, and with stirring at 15° to 20° C., a solution prepared from 2.04 g (0.02 mole) of DL-α-amino-n-butyric acid, 1.12 g (0.02 mole) of potassium hydroxide and 40 ml of water was added dropwise over the period of 5 minutes. The mixture was then sitrred at 30° C. for 30 minutes. After the reaction, the reactor was cooled with ice, and in the meanwhile, 2 ml of conc. hydrochloric acid was added to the reaction solution. The solution was then extracted with 100 ml of toluene. The toluene layer was washed with 50 ml of a saturated aqueous solution of sodium chloride and 50 ml of water, and the solvent was removed by concentration under reduced pressure to afford a yellowish white solid. Recrystallization of the solid from ethanol afforded 2.63 g (yield 86%) of 2,3-dicyano-5-(1-carboxy-n-propyl)amino-6-phenylpyrazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04460403 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-c4bcc439df9f499ebd2d096aaedeeb85 |
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| Source note | uspto-grants-1984_07 |
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