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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2303생성일: 2026년 10월 23일

2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol → 2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanol

https://huagongshe.com/ko/reaction/2303

반응식

참여 물질

역할이름HCID투입량
반응물2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanolHCID 11807790—
촉매HCID 178418390HCID 178418390—
용매EthanolHCID 702—
생성물2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanolHCID 1111829789.7%

반응 단계

A mixture of 2-{6-azido-5-(4-methylphenyl)pyrimidin-4-yloxy}-ethanol (19.6 g), 10% palladium-carbon (50% moist) (4.0 g) and ethanol (240 ml) is subjected to catalytic hydrogenation at room temperature under hydrogen atmosphere (1 atm) for one hour. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is recrystallized from ethyl acetate/n-hexane to give 2-{6-amino-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (15.9 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728706
출처 데이터셋uspto-grants-1998_03
ORD IDord-5cec6056ae4c4169bd4252bc117b2be6
출처 메모uspto-grants-1998_03