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HRID 1828541생성일: 2026년 10월 23일

N-(4-methyl-5-nitropyridin-2-yl)acetamide → N-(5-Amino-4-methylpyridin-2-yl)acetamide

https://huagongshe.com/ko/reaction/1828541

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-methyl-5-nitropyridin-2-yl)acetamideHCID 13567013—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N-(5-Amino-4-methylpyridin-2-yl)acetamideHCID 22063573103%

반응 단계

The N1-(4-methyl-5-nitro-2-pyridyl)acetamide (4.70 g, 24.1 mmol) obtained in (A) was dissolved in ethanol (150 ml), added with 10% palladium/carbon (0.95 g) and subjected to catalytic reduction overnight at 1 atm under hydrogen atmosphere. The catalyst was removed by filtration and washed with ethanol. The filtrate was concentrated and the resulting residue was purified by silica gel column chromatography (chloroform chloroform:methanol=100:5) to obtain the title compound (4.10 g, quantitative) as brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07056917B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-ef9681cf549f4b29a9a1e54462238dc5
출처 메모uspto-grants-2006_06