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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374145Generated: October 25, 2026

3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester → N-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamide

https://huagongshe.com/reaction/374145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Nitroxypropylamine nitrateHCID 22014591—
SolventMethanolHCID 887—
ProductN-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamideHCID 1039979439%

Reaction Steps

Isopropyl N-cyano-3-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 (0.16 g, 2.9 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, and the residue was extracted with chloroform (30 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrated residue thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C-200, 30 g) eluting with chloroform-methanol (60:1). Eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.26 g, 1.0 mmol, yield: 39%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166347
Source datasetuspto-grants-1992_11
ORD IDord-d14fe50d3e4047a8a3e294f045a77354
Source noteuspto-grants-1992_11