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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374166Generated: October 28, 2026

Benzhydrylamine → N-cyano-N'-diphenylmethyl-3-pyridinecarboximidamide

https://huagongshe.com/reaction/374166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
Reactant3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
SolventMethanolHCID 887—
ProductN-cyano-N'-diphenylmethyl-3-pyridinecarboximidamideHCID 1973450758%

Reaction Steps

Isopropyl N-cyano-3-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and aminodiphenylmethane (0.54 g, 2.9 mmol) was added. The mixture was stirred at room temperature for 1 hour. 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, 40 g) eluting with chloroform-methanol (100:1). The eluted fractions were concentrated under reduced pressure to give N-cyano-N'-diphenylmethyl-3-pyridinecarboximidamide (0.48 g, 1.5 mmol, yield: 58%) as colorless syrup. Next, to this syrup was added a solution of 5% hydrogen chloride in methanol (2 ml) to form a solution. The solution was further crystallized from methanol-diethyl ether to give N-cyano-N'-diphenylmethyl-3-pyridinecarboximidamide hydrochloride as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166347
Source datasetuspto-grants-1992_11
ORD IDord-75d2c385a8ff405fbc35a3f62ebb1868
Source noteuspto-grants-1992_11