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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327117Generated: October 25, 2026

1,2-Diphenylethylamine → N-cyano-N'-(1,2-diphenylethyl)-3-pyridinecarboximidamide

https://huagongshe.com/reaction/327117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiphenylethylamineHCID 26482—
Reactant3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
SolventMethanolHCID 887—
ProductN-cyano-N'-(1,2-diphenylethyl)-3-pyridinecarboximidamideHCID 1973454858%

Reaction Steps

Isopropyl N-cyano-3-pyridinecarboximidate (0.60 g, 3.2 mmol) was dissolved in methanol (10 ml), and 1,2-diphenylethylamine (0.69 g, 3.5 mmol) was added. The mixture was stirred at room temperature for 45 minutes. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (100:1). The eluted fractions were concentrated under reduced pressure to give N-cyano-N'-(1,2-diphenylethyl)-3 pyridinecarboximidamide (0.60 g, 1.8 mmol, yield: 58%) as colorless syrup. Next, to this syrup was added a 5% hydrogen chloride solution in methanol (2.5 ml). The solution was crystallized from methanol-diethyl ether to give N-cyano-N'-(1,2-diphenylethyl)-3-pyridinecarboximidamide hydrochloride as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272164
Source datasetuspto-grants-1993_12
ORD IDord-cbb066c65fe94e858d62ddb9d33c4ffa
Source noteuspto-grants-1993_12