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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1384226생성일: 2026년 10월 27일

Sodium Methoxide → 2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide

https://huagongshe.com/reaction/1384226

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참여 물질

역할이름HCID투입량
반응물Sodium MethoxideHCID 10942334—
반응물Methyl 4-(3-{[(3-Methoxy-5-Methylpyrazin-2-yl)[(2-Methylpropoxy)carbonyl]aMino]sulfonyl}pyridin-2-yl)benzoateHCID 22325614—
용매MethanolHCID 887—
생성물2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamideHCID 2118631228.4%

반응 단계

A solution of N-(isobutoxycarbonyl)-2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (830 mg) and sodium methoxide (433 mg) in methanol (25 ml) was heated under reflux for 1 hour. Volatile material was removed by evaporation and saturated ammonium chloride solution (20 ml) was added to the residue. The mixture was extracted with ethyl acetate (2×20 ml) and the extracts were washed with water (2×15 ml) and dried (MgSO4). The solvent was removed by evaporation and the residue was purified by flash chromatography, eluting with 25-50% ethyl acetate/hexane, to give 2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (190 mg), m.p. 144-146° C.; microanalysis found: C, 55.2; H, 4.3; N, 13.3%; C23H24BrN4O4S requires: C, 55.1; H, 4.4; N, 13.5%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06258817B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-beea5354b3554ea49b25e8a6f34be7ca
출처 메모uspto-grants-2001_07