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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259643생성일: 2026년 10월 25일

Water → 3-(4-Methylpiperazin-1-yl)carbonyloxy-2-(1,5-naphthyridin-2-yl)isoindolin-1-one

https://huagongshe.com/reaction/259643

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-Methyl-1-piperazinecarbonyl chlorideHCID 3016935—
반응물3-Hydroxy-2-(1,5-naphthyridin-2-yl)isoindolin-1-oneHCID 21422083—
용매DimethylformamideHCID 6228—
생성물3-(4-Methylpiperazin-1-yl)carbonyloxy-2-(1,5-naphthyridin-2-yl)isoindolin-1-oneHCID 2144438656%

반응 조건

온도13 °C

반응 단계

A suspension of sodium hydride (50% dispersion in mineral oil) (1.46 g.) in anhydrous dimethylformamide (80 cc.) is added to a suspension of 3-hydroxy-2-(1,5-naphthyridin-2-yl)isoindolin-1-one (7 g.) in anhydrous dimethylformamide (410 cc.). When the evolution of gas has ceased, a solution of 1-chlorocarbonyl-4-methyl-piperazine (4.6 g.) in anhydrous dimethylformamide (25 cc.) is added dropwise. After stirring for 4 hours, the reaction mixture is poured into water (3,000 cc.) cooled to 13° C. The precipitate is filtered off, washed with water (75 cc.) and then dried to yield 3-(4-methylpiperazin-1-yl)carbonyloxy-2-(1,5-naphthyridin-2-yl) isoindolin-1-one (5.7 g.) melting at 170°-171° C. After recrystallisation from acetonitrile (50 cc.), the products melts at 173° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04038391
출처 데이터셋uspto-grants-1977_07
ORD IDord-43644f201fec460e86b259fed13f4637
출처 메모uspto-grants-1977_07