Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAlpha-Aminobutyric AcidHCID 6657—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Chloro-6-phenylpyrazine-2,3-dicarbonitrileHCID 12907205—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,3-Dicyano-5-(1-carboxy-n-propyl)amino-6-phenylpyrazineHCID 1333697086%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460403
Source datasetuspto-grants-1984_07
ORD IDord-c4bcc439df9f499ebd2d096aaedeeb85
Source noteuspto-grants-1984_07