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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519671생성일: 2026년 10월 26일

Ethanol → N-hydroxy-2-[{[4'-(methoxymethyl)biphenyl-4-yl]carbonyl}(methyl)amino]-N'-methylpropanediamide

https://huagongshe.com/reaction/1519671

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물HydroxylamineHCID 787—
반응물4-(Methoxymethyl)-4'-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}biphenylHCID 71268148—
용매TetrahydrofuranHCID 8028—
생성물N-hydroxy-2-[{[4'-(methoxymethyl)biphenyl-4-yl]carbonyl}(methyl)amino]-N'-methylpropanediamideHCID 8667925446%

반응 단계

Ethanol (5.0 mL) and a 50% aqueous solution (5.0 mL) of hydroxylamine were added to a tetrahydrofuran (5.0 mL) solution of 4-(methoxymethyl)-4′-{[1-methoxy-3-(methylamino)-1,3-dioxopropan-2-yl](methyl)carbamoyl}biphenyl (0.40 g) as obtained in Example 3-(4), and the mixture was stirred for 2 hours at room temperature. Then, the reaction mixture was concentrated under reduced pressure, and purified by preparative silica gel thin-layer chromatography (chloroform/methanol=85/15). IPE was added, and the precipitated solid was filtered off and dried to obtain N-hydroxy-2-[{[4′-(methoxymethyl)biphenyl-4-yl]carbonyl}(methyl)amino]-N′-methylpropanediamide (Compound 4, pink solid) (0.18 g, 46%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073821B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-a96a4c7e3f7f4f9cb4a795bcc037349a
출처 메모uspto-grants-2015_07