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HRID 637501作成日:2026年10月25日

Propionamide → Ethyl isocyanate

https://huagongshe.com/reaction/637501

反応式

関与物質

役割名称HCID仕込み量
反応物PropionamideHCID 6578—
反応物TriethylamineHCID 8471—
反応物1,2-Dihydropyrazin-2-oneHCID 72758—
反応物5-(4-Aminophenyl)-2(1H)-pyrazinone hydrochlorideHCID 19794232—
溶媒DimethylformamideHCID 6228—
生成物Ethyl isocyanateHCID 8022—
生成物N-Ethyl-N'-[4-(5-oxo-4,5-dihydropyrazin-2-yl)phenyl]ureaHCID 13853579—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556711
出典データセットuspto-grants-1985_12
ORD IDord-dabd43733173444fae1efc4adbff2f50
出典メモuspto-grants-1985_12