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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327105Generated: October 25, 2026

Triethylamine → N-cyano-N'-(4-nitrobenzyl)-3-pyridinecarboximidamide

https://huagongshe.com/reaction/327105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
Reactant4-Nitrobenzylamine hydrochlorideHCID 11252467—
SolventMethanolHCID 887—
ProductN-cyano-N'-(4-nitrobenzyl)-3-pyridinecarboximidamideHCID 1973449596.2%

Reaction Steps

Isopropyl N-cyano-3-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (5 ml), and a solution of p-nitrobenzylamine hydrochloride (0.55 2.9 mmol) and triethylamine (0.32 g, 3.2 mmol) in methanol (5 ml) was added. The mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and the concentrated residue thus obtained was crystallized from methanol-diethyl ether to give the title compound (0.70 g, 2.5 mmol, yield: 95%) as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272164
Source datasetuspto-grants-1993_12
ORD IDord-303f0471ed9842b0a8abf3171c649631
Source noteuspto-grants-1993_12