戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 577834作成日:2026年10月25日

2-Pyrazinecarboxylic acid → N-Methoxy-N-methylpyrazine-2-carboxamide

https://huagongshe.com/reaction/577834

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TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-Methoxy-N-methylpyrazine-2-carboxamideHCID 2261313192.2%

反応手順

To a 500 ml round bottom flask, pyrazine-2-carboxylic acid (58 g, 467.37 mmol) was suspended in dry CH2Cl2 (250 ml): oxalyl chloride (50.1 ml, 560.85 mmol) was added along with a few drops of DMF, and the mixture was stirred at room temperature for 12 hours. N,O-Dimethylhydroxylamine hydrochloride (54.7 g, 560.85 mmol) was added, and the resultant mixture was cooled down to 5° C. Triethylamine (195 ml, 1402.12 mmol) was added via a dropping funnel, and the reaction mixture was stirred at room temperature for 30 minutes before being filtered. The filter cake was washed with EtOAc, and the combined filtrate was washed with saturated sodium bicarbonate and brine, concentrated to an oil and dried under high vacuum to give the desired product (72 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040528B2
出典データセットuspto-grants-2015_05
ORD IDord-720c37ba76b24097a3fe2d41606ddc87
出典メモuspto-grants-2015_05