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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374186Generated: October 25, 2026

Triethylamine → N-cyano-N'-(2-nitroxyethyl)pyrazinecarboximidamide

https://huagongshe.com/reaction/374186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanol, 2-amino-, 1-nitrate, nitrate (1:1)HCID 78397—
ReactantMethyl N-cyanopyrazinecarboximidateHCID 10057818—
SolventMethanolHCID 887—
ProductN-cyano-N'-(2-nitroxyethyl)pyrazinecarboximidamideHCID 1033165226%

Reaction Steps

Methyl N-cyanopyrazinecarboximidate (0.49 g, 3.0 mmol) was dissolved in methanol (6 ml), 2-nitroxyethylamine nitrate (1.01 g, 6.0 mmol) and triethylamine (1.01 g, 10.0 mmol) were added. The mixture was stirred at room temperature for 46 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and the residue thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C 200, 30 g) eluting with chloroform-methanol (300:1). The eluted fractions were concentrated under reduced pressure and crystallized from diethyl ether to give the title compound (0.18 g, 0.78 mmol, yield: 26%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166347
Source datasetuspto-grants-1992_11
ORD IDord-c8529e887c1041cf90a5fa40260146ca
Source noteuspto-grants-1992_11