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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577834Generated: October 27, 2026

2-Pyrazinecarboxylic acid → N-Methoxy-N-methylpyrazine-2-carboxamide

https://huagongshe.com/reaction/577834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrazinecarboxylic acidHCID 1047—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-Methoxy-N-methylpyrazine-2-carboxamideHCID 2261313192.2%

Reaction Steps

To a 500 ml round bottom flask, pyrazine-2-carboxylic acid (58 g, 467.37 mmol) was suspended in dry CH2Cl2 (250 ml): oxalyl chloride (50.1 ml, 560.85 mmol) was added along with a few drops of DMF, and the mixture was stirred at room temperature for 12 hours. N,O-Dimethylhydroxylamine hydrochloride (54.7 g, 560.85 mmol) was added, and the resultant mixture was cooled down to 5° C. Triethylamine (195 ml, 1402.12 mmol) was added via a dropping funnel, and the reaction mixture was stirred at room temperature for 30 minutes before being filtered. The filter cake was washed with EtOAc, and the combined filtrate was washed with saturated sodium bicarbonate and brine, concentrated to an oil and dried under high vacuum to give the desired product (72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040528B2
Source datasetuspto-grants-2015_05
ORD IDord-720c37ba76b24097a3fe2d41606ddc87
Source noteuspto-grants-2015_05