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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259652생성일: 2026년 10월 23일

Piperazine → 2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(piperazin-1-yl)carbonyloxy-isoindolin-1-one

https://huagongshe.com/ko/reaction/259652

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물Diisopropyl EtherHCID 7914—
반응물2-(7-Chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-1-isoindolinoneHCID 23343637—
용매AcetonitrileHCID 6342—
생성물2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(piperazin-1-yl)carbonyloxy-isoindolin-1-oneHCID 2334363947%

반응 단계

Anhydrous piperazine (5.15 g.) is added to a suspension of 2-(7-chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one (5.2 g.) in acetonitrile (32 cc.). The reaction mixture is stirred for 1 hour at a temperature of about 20° C. and diisopropyl ether (150 cc.) is then added. The insoluble product is filtered off and washed with a mixture (20 cc.) of acetonitrile and diisopropyl ether (50--50 by volume) and then with diisopropyl ether (50 cc.). After recrystallisation of the product thus obtained from a mixture (160 cc.) of acetonitrile and methanol (90- 10 by volume), 2-(7-chloro-1,8-naphthyridin-2-yl)-3-(piperazin-1-yl)carbonyloxy-isoindolin-1-one (2.4 g.), melting with decomposition at 245° C., is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04038391
출처 데이터셋uspto-grants-1977_07
ORD IDord-9b564f632d694613a2f8f05d8754c4f4
출처 메모uspto-grants-1977_07