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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1588540Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1588540

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DiphenylethylamineHCID 26482—
Edukt3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
LösungsmittelMethanolHCID 887—
ProduktN-cyano-N'-(1,2-diphenylethyl)-3-pyridinecarboximidamideHCID 1973454858%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05223508
Quelldatensatzuspto-grants-1993_06
ORD IDord-f2c1281b52de4a81925814674fea22ff
Quellennotizuspto-grants-1993_06