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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374173Erstellt: 24. Oktober 2026

Isopropyl N-cyano-4-pyridinecarboximidate → N-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamide

https://huagongshe.com/de/reaction/374173

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropyl N-cyano-4-pyridinecarboximidateHCID 10012715—
EduktSodium MethoxideHCID 10942334—
Edukt3-Nitroxypropylamine nitrateHCID 22014591—
LösungsmittelMethanolHCID 887—
ProduktN-cyano-N'-(3-nitroxypropyl)-4-pyridinecarboximidamideHCID 1003767641,5%

Reaktionsschritte

Isopropyl N-cyano-4-pyridinecarboximidate (0.50 g, 2.6 mmol) was dissolved in methanol (10 ml), and 3-nitroxypropylamine nitrate (0.53 g, 2.9 mmol) and sodium methoxide (0.22 g, 4.1 mmol) were added. The mixture was stirred at room temperature for 18 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The residual concentrate was extracted with chloroform (50 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residual concentrate was subjected to chromatography on a silica gel column (WAKO GEL C-200, 50 g) eluting with chloroform-methanol (60:1). The eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.27 g, 1.08 mmol, yield: 41%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166347
Quelldatensatzuspto-grants-1992_11
ORD IDord-af49dd18063e4be799d543e2d517d44b
Quellennotizuspto-grants-1992_11