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HRID 393573作成日:2026年10月23日

2-Pyrazinecarboxylic acid → Pyrazinamide

https://huagongshe.com/ja/reaction/393573

反応式

関与物質

役割名称HCID仕込み量
反応物2-Pyrazinecarboxylic acidHCID 1047—
反応物N,N-DiethylanilineHCID 7061—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒TetrahydrofuranHCID 8028—
生成物PyrazinamideHCID 1046425.5%

反応条件

温度23 °C

反応手順

Diethylaniline (0.33 μL, 2.1 μmol, 1.1 equiv) was added in one portion to a stirred solution of the amine (1.0 mg, 1.9 μmol, 1 equiv) in THF (0.2 mL) at 0° C. under an argon atmosphere and the solution was stirred for 5 min. 2-Pyrazinecarboxylic acid (0.31 mg, 2.5 μmol, 1.3 equiv), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.48 mg, 2.5 μmol, 1.3 equiv) and 1-hydroxybenzotriazole (0.31 mg, 2.3 μmol, 1.2 equiv) were then added separately, each in one portion, to the above solution at 0° C. The reaction mixture was warmed to 23° C. over 17 h 40 min, then was quenched with saturated aqueous ammonium chloride solution (3 mL). The mixture was diluted with ethyl acetate (10 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (10 mL) and the combined organic layer was dried over sodium sulfate. Concentration in vacuo left a white solid, which was purified by flash column chromatography (80% ethyl acetate-hexanes) to give the pyrazine-2-carboxylic acid amide derivative (1.1 mg, 92%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809099B2
出典データセットuspto-grants-2004_10
ORD IDord-50c74831cfcb4e1e8ad6295c27f1b427
出典メモuspto-grants-2004_10