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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259644생성일: 2026년 10월 24일

Hexamethylphosphoramide → 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4-methylpiperazin-1-yl)carbonyloxy-isoindolin-1-one

https://huagongshe.com/ko/reaction/259644

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylphosphoramideHCID 12679—
반응물Sodium hydrideHCID 24758—
반응물4-Methyl-1-piperazinecarbonyl chlorideHCID 3016935—
반응물2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinoneHCID 14182181—
용매DimethylformamideHCID 6228—
생성물2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4-methylpiperazin-1-yl)carbonyloxy-isoindolin-1-oneHCID 2142210945.9%

반응 단계

Sodium hydride (50% dispersion in mineral oil) (0.8 g.) is added to a suspension of 2-(7-methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-isoindolin-1-one (4.63 g.) in anhydrous dimethylformamide (45 cc.), whilst keeping the temperature between 18°-20° C. The reaction mixture is stirred for a further 4 hours 30 minutes. A solution of 1-chlorocarbonyl-4-methylpiperazine (2.7 g.) in anhydrous dimethylformamide (25 cc.) is then added over the course of 15 minutes and at a temperature of 20° C. The suspension is stirred for 17 hours at a temperature of about 20° C., and then anhydrous hexamethylphosphotriamide (7 cc.) is added. After 15 minutes, the reaction mixture is poured into ice-water (500 g.). The precipitate is filtered off and washed with water (45 cc.). A product (6.1 g.) is obtained and is recrystallised from diisopropyl ether (1,500 cc.). 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4 -methylpiperazin-1-yl)carbonyloxy-isoindolin-1-one (3 g.), melting at 191° C., is thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04038391
출처 데이터셋uspto-grants-1977_07
ORD IDord-f6d9a6c5b14e4618a54b3b7e9798e706
출처 메모uspto-grants-1977_07