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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 374145Erstellt: 24. Oktober 2026

3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl ester → N-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamide

https://huagongshe.com/de/reaction/374145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Pyridinecarboximidic acid, N-cyano-, 1-methylethyl esterHCID 10081201—
EduktSodium MethoxideHCID 10942334—
Edukt3-Nitroxypropylamine nitrateHCID 22014591—
LösungsmittelMethanolHCID 887—
ProduktN-cyano-N'-(3-nitroxypropyl)-3-pyridinecarboximidamideHCID 1039979439%

Reaktionsschritte

Isopropyl N-cyano-3-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 (0.16 g, 2.9 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, and the residue was extracted with chloroform (30 ml×3). The chloroform layer was washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrated residue thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C-200, 30 g) eluting with chloroform-methanol (60:1). Eluted fractions were concentrated under reduced pressure and crystallized from methanol-diethyl ether to give the title compound (0.26 g, 1.0 mmol, yield: 39%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05166347
Quelldatensatzuspto-grants-1992_11
ORD IDord-d14fe50d3e4047a8a3e294f045a77354
Quellennotizuspto-grants-1992_11