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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986113Generated: October 28, 2026

Triethylamine → 3-Chloro-N-(2,4-difluorophenyl)pyrazine-2-carboxamide

https://huagongshe.com/reaction/1986113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DifluoroanilineHCID 9709—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Chloro-2-pyrazine-carboxylic acidHCID 1501900—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Chloro-N-(2,4-difluorophenyl)pyrazine-2-carboxamideHCID 5772136253.6%

Reaction Steps

To a mixture of 3-chloropyrazine-2-carboxylic acid (Tyger Scientific, 500 mg, 3.15 mmol) in methylene chloride (30 mL) and DMF (0.1 mL) was added oxalyl chloride (593 mg, 4.7 mmol). After stirring 30 min the reaction mixture was concentrated in vacuo. The residue was taken up in acetonitrile (12 mL) and was treated with triethylamine (920 mg, 9.1 mmol) and 2,4-difluoroaniline (430 mg, 3.3 mmol) and stirred 30 min. The reaction mixture was partitioned between ethyl acetate and brine. The organic layer was washed with brine, dried over anhydrous MgSO4, and then concentrated in vacuo. The resulting solid was recrystallized (ethyl acetate/hexanes) to give the amide (455 mg, 53%) as a solid. MS(ESI+) m/z 270 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547782B2
Source datasetuspto-grants-2009_06
ORD IDord-7933e29711dd45609b0a8e7d05c8dd98
Source noteuspto-grants-2009_06