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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100348Generated: October 27, 2026

Oxalyl chloride → N-(6-Amino-5-chloropyrazin-2-yl)-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/2100348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
Reactant3-Chloropyrazine-2,6-diamineHCID 12101492—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(6-Amino-5-chloropyrazin-2-yl)-1-methyl-1H-pyrazole-5-carboxamideHCID 5779915135.7%

Reaction Steps

Oxalyl chloride (0.288 ml, 3.32 mmol) was added to a suspension of 1-methyl-1H-pyrazole-5-carboxylic acid (0.279 g, 2.21 mmol) in dichloromethane (5 ml) followed by 1 drop of dimethylformamide. The mixture was stirred at room temperature for 4 hours before concentrating in vacuo and azeotroping with dichloromethane. The residue was taken up in pyridine (1 ml) and added to a solution of 3-chloro-pyrazine-2,6-diamine (Preparation 1) (0.16 g, 1.11 mmol) and the mixture heated at 60° C. for 3 hours before cooling to room temperature and concentrating in vacuo. The residue was purified by silica gel column chromatography, eluting with ethylacetate:heptane 1:1, to afford the product as a pale solid (100 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572797B2
Source datasetuspto-grants-2009_08
ORD IDord-9556d7f98ff5494b93ee7fa2fd9ed7d8
Source noteuspto-grants-2009_08