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HRID 81476作成日:2026年10月26日

3-Amino-2-pyrazinecarboxylic acid → 3-Amino-pyrazine-2-carboxylic acid methoxy-methylamide

https://huagongshe.com/reaction/81476

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-2-pyrazinecarboxylic acidHCID 72656—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物DiisopropylethylamineHCID 81531—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒DimethylformamideHCID 6228—
生成物3-Amino-pyrazine-2-carboxylic acid methoxy-methylamideHCID 86634549—

反応手順

To a solution of 3-aminopyrazine-2-carboxylic acid (1 g, 7.2 mmol) in DMF (15 ml) is added EDC hydrochloride (1.7 g, 8.6 mmol), HOBt (1.16 g, 8.6 mmol), diisopropylethylamine (3.08 ml, 18 mmol) and N-methoxy-N-methylamine hydrochloride (0.84 g, 8.6 mmol), and the resulting solution is stirred at room temperature for 15 hours. The reaction is concentrated in vacuo, and sat. aq. NaHCO3 (50 ml) is added to the residue. The product is extracted into EtOAc (3×60 ml), washed with sat. aq. NaCl (2×50 ml), dried (MgSO4) and concentrated in vacuo to afford a yellow residue. Purification by flash chromatography (SiO2, 0-5% MeOH in DCM) yields 3-amino-pyrazine-2-carboxylic acid methoxy-methylamide as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846687B2
出典データセットuspto-grants-2014_09
ORD IDord-64858c2c746d45169a84ce8da8f2785a
出典メモuspto-grants-2014_09