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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327122Generated: October 25, 2026

Isopropyl N-cyano-4-pyridinecarboximidate → N-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamide

https://huagongshe.com/reaction/327122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl N-cyano-4-pyridinecarboximidateHCID 10012715—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Nitroxypropylamine nitrateHCID 22014591—
SolventMethanolHCID 887—
ProductN-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamideHCID 1003767641.5%

Reaction Steps

Isopropyl N-cyano-4-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and 3-nitroxypropylamine nitrate (0.53 g, 2.9 mmol) and sodium methoxide (0.22 g, 4.1 mmol) were added. The mixture was stirred at room temperature for 18 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate was extracted with chloroform (50 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (60:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.27 g, 1.08 mmol, yield: 41%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272164
Source datasetuspto-grants-1993_12
ORD IDord-18f7a44a8d9e4081a4f957a470fd5d06
Source noteuspto-grants-1993_12