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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326861Generated: October 30, 2026

3-Aminopyrazine-2-carbonitrile → HCID 10850551, compound

https://huagongshe.com/reaction/326861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminopyrazine-2-carbonitrileHCID 817699—
ReactantHCID 18967941HCID 18967941—
SolventEthanolHCID 702—
ProductHCID 10850551HCID 10850551—

Reaction Steps

A suspension of 2.3 g (0.019 mole) of 3-amino-2-pyrazinecarbonitrile and 5.2 g (0.029 mole) of 2-(benzylthio)acetamidine [prepared according to J. M. McManus, J. Heterocycl. Chem. 1968, 5, 137] in 150 ml of absolute ethanol is refluxed for 2 hours. After cooling, the solution obtained is concentrated to dryness under reduced pressure. The residue is washed with isopropyl ether and dried under reduced pressure. An amorphous solid is obtained, and is used in the next step without further purification. Yld: 5.4 g (quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270465
Source datasetuspto-grants-1993_12
ORD IDord-bfea307082de46eba2a15c650f417e6f
Source noteuspto-grants-1993_12