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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542465Erstellt: 25. Oktober 2026

Propionamide → Ethyl isocyanate

https://huagongshe.com/reaction/542465

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropionamideHCID 6578—
EduktTriethylamineHCID 8471—
Edukt1,2-Dihydropyrazin-2-oneHCID 72758—
Edukt5-(4-Aminophenyl)-2(1H)-pyrazinone hydrochlorideHCID 19794232—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl isocyanateHCID 8022—
ProduktN-Ethyl-N'-[4-(5-oxo-4,5-dihydropyrazin-2-yl)phenyl]ureaHCID 13853579—

Reaktionsschritte

5-(4-Aminophenyl)-2(1H)-pyrazinone hydrochloride (1.5 g) was suspended in dimethylformamide (20 ml) and triethylamine (3 ml) was added. The dark solution was filtered. Ethyl isocyanate (0.53 ml) was prepared by slowly adding lead tetra acetate (7.3 g) to a solution of propionamide (1.2 g) in dimethylformamide (50 ml). The solution was initially blood-red, but after stirring for one hour at room temperature it turned colourless. The solution of pyrazinone was added and the mixture stirred at room temperature for 36 hours. It was evaporated to dryness and the residue was washed with water; the resulting orange solid was collected by filtration. Recrystallization from glacial acetic acid afforded the title compound; m.p. >300° C.; νmax (liquid paraffin) 1660, 1640 cm-1 ; δ (DMSO-d6) 1.07 (t, 3H, CH3), 6.05 (t, 1H, --NHEt), 7.93, 8.08 (2d, 2H, pyridine H's).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04657906
Quelldatensatzuspto-grants-1987_04
ORD IDord-f806cdb2a6044250a09221ef9eec01a9
Quellennotizuspto-grants-1987_04