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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1719065생성일: 2026년 10월 25일

Hydroxyamine hydrochloride → 6-ethyl-5-(4-isopropoxyphenyl)-3-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-2-propylpyrimidin-4(3H)-one

https://huagongshe.com/reaction/1719065

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참여 물질

역할이름HCID투입량
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Sodium BicarbonateHCID 516892—
반응물4'-{[4-ethyl-5-(4-isopropoxyphenyl)-6-oxo-2-propylpyrimidin-1(6H)-yl]methyl}biphenyl-2-carbonitrileHCID 57460419—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물6-ethyl-5-(4-isopropoxyphenyl)-3-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-2-propylpyrimidin-4(3H)-oneHCID 13602696979%

반응 조건

온도90 °C

반응 단계

4′-{[4-Ethyl-5-(4-isopropoxyphenyl)-6-oxo-2-propylpyrimidin-1(6H)-yl]methyl}biphenyl-2-carbonitrile (0.5 g) was dissolved in dimethyl sulfoxide (5 mL), and hydroxylamine hydrochloride (0.71 g) and sodium hydrogen carbonate (1 g) were added. The mixture was stirred overnight at 90° C. After cooling, the reaction mixture was diluted with ethyl acetate, washed with water, dried over sodium sulfate and concentrated. The residue was dissolved in tetrahydrofuran (5 mL), and N,N′-carbonyldiimidazole (0.25 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.23 mL) were added. After stirring for 30 min, the reaction mixture was diluted with ethyl acetate, washed with 1 M hydrochloric acid, dried over sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.44 g, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07803940B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-75a805e878e64dffa3e5e29b32204892
출처 메모uspto-grants-2010_09