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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49451생성일: 2026년 10월 23일

2-Pyridinecarboxamide → N-(3-hydroxy-4-methoxy-2-pyridylcarbonyl)-2-amino-2-deoxy-alpha-D-glucopyranose

https://huagongshe.com/ko/reaction/49451

반응식

참여 물질

역할이름HCID투입량
반응물2-PyridinecarboxamideHCID 15070—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물3-Hydroxy-4-methoxypyridine-2-carboxylic acidHCID 11041121—
반응물[(3S,7R,8R,9S)-7-benzyl-8-hydroxy-9-methyl-2,6-dioxo-[1,5]dioxonane-3-yl]-carbamic acid tert-butyl esterHCID 69151164—
용매MethanolHCID 887—
생성물N-(3-hydroxy-4-methoxy-2-pyridylcarbonyl)-2-amino-2-deoxy-alpha-D-glucopyranoseHCID 1868167888%

반응 단계

1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-alpha-D-glucopyranose (151) and 3-hydroxy-4-methoxypicolinic acid were coupled together using standard coupling procedure C. To a solution of the resulting picolinamide (0.19 g, 0.38 mmol) in 6 mL of methanol was added lithium hydroxide monohydrate (0.92 mmol, 40 mg). The reaction mixture was stirred at room temperature overnight. The solution was neutralized by the addition of DOWEX® 5×8-100 acidic resin (0.5 g). The mixture was filtered and concentrated to afford the title compound (110 mg, 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706740B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d6fa8b29480741348e488d2b098d95b7
출처 메모uspto-grants-2004_03