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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355367Generated: October 30, 2026

Ethanolamine → 3-Bromo-5-[(2-hydroxyethyl)amino]-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/1355367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromo-5-chloropyrazine-2-carbonitrileHCID 18753200—
Solvent1,4-DioxaneHCID 31275—
Product3-Bromo-5-[(2-hydroxyethyl)amino]-2-pyrazinecarbonitrileHCID 1875320553.9%

Reaction Steps

0.061 g (1.00 mmol) of ethanolamine were added slowly at room temperature to a solution of 0.218 g (1.0 mmol) of the 3-bromo-5-chloro-pyrazine-2-carbonitrile and 0.264 g (2.0 mmol) of N-ethyldiisopropylamine in 15.0 ml of dioxane. The reaction mixture was stirred at room temperature for 18 hours. It was subsequently poured into 50 ml of an ice/water/sodium hydrogen carbonate mixture and extracted 3 times with 50 ml of ethylacetate. The combined ethylacetate phases were dried over magnesium sulfate and evaporated under reduced pressure. The residue formed was chromatographed on silica gel with a 100:0 to 95:5 v/v gradient of dichloromethane and methanol as the eluent giving 0.131 g (0.539 mmol, 53.9% of theory) of the 3-bromo-5-(2-hydroxy-ethylamino)-pyrazine-2-carbonitrile as yellow amorphous solid; MS: 243 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586422B2
Source datasetuspto-grants-2003_07
ORD IDord-2f1452df23274beb864e4636881dd501
Source noteuspto-grants-2003_07