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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81476생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/81476

반응식

참여 물질

역할이름HCID투입량
반응물3-Amino-2-pyrazinecarboxylic acidHCID 72656—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
생성물3-Amino-pyrazine-2-carboxylic acid methoxy-methylamideHCID 86634549—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846687B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-64858c2c746d45169a84ce8da8f2785a
출처 메모uspto-grants-2014_09