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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519674생성일: 2026년 10월 26일

Ethanol → N-hydroxy-N'-methyl-2-[methyl({4'-[3-(morpholin-4-yl)propoxy]biphenyl-4-yl}carbonyl)amino]propanediamide

https://huagongshe.com/reaction/1519674

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참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물HydroxylamineHCID 787—
반응물4-{3-[(4'-{[1-Methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}biphenyl-4-yl)oxy]propyl}morpholineHCID 71268168—
용매TetrahydrofuranHCID 8028—
생성물N-hydroxy-N'-methyl-2-[methyl({4'-[3-(morpholin-4-yl)propoxy]biphenyl-4-yl}carbonyl)amino]propanediamideHCID 8667925539%

반응 단계

Ethanol (1.0 mL) and a 50% aqueous solution (1.0 mL) of hydroxylamine were added to a THF (1.0 mL) solution of 4-{3-[(4′-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}biphenyl-4-yl)oxy]propyl}morpholine (0.11 g) as obtained in Example 4-(4), and the mixture was stirred for 2 hours at room temperature. Then, the reaction mixture was concentrated under reduced pressure. The resulting residue was purified by preparative silica gel thin-layer chromatography (chloroform/methanol=90/10), and then recrystallized from ethyl acetate/hexane to obtain N-hydroxy-N′-methyl-2-[methyl({4′-[3-(morpholin-4-yl)propoxy]biphenyl-4-yl}carbonyl)amino]propanediamide (Compound 7, light brown solid) (43 mg, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073821B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-b364439ceb58472f87a0ff06ea1fe8a9
출처 메모uspto-grants-2015_07