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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327126Generated: October 27, 2026

Phenyl-2-aminoethyl sulfide → N-cyano-N'-(2-phenylthioethyl)-4-pyridinecarboximidamide

https://huagongshe.com/reaction/327126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl-2-aminoethyl sulfideHCID 37013—
ReactantIsopropyl N-cyano-4-pyridinecarboximidateHCID 10012715—
SolventMethanolHCID 887—
ProductN-cyano-N'-(2-phenylthioethyl)-4-pyridinecarboximidamideHCID 1973456866%

Reaction Steps

Isopropyl N-cyano-4-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (5 ml), and 2-phenylthioethylamine (0.49 g, 3.2 mmol) 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 residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 10 g) eluting with chloroform-methanol (50:1). The eluted fractions were concentrated under reduced pressure and crystallized from diethyl ether to give the title compound (0.49 g, 1.7 mmol, yield: 66%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272164
Source datasetuspto-grants-1993_12
ORD IDord-358eb9e37feb4c008aeed5bfc85eaaf2
Source noteuspto-grants-1993_12