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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46807생성일: 2026년 10월 24일

(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol → Quinidinone

https://huagongshe.com/ko/reaction/46807

반응식

참여 물질

역할이름HCID투입량
반응물(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanolHCID 5953—
반응물SodiumHCID 5360545—
반응물FluoreneoneHCID 22281833—
용매TolueneHCID 1140—
생성물QuinidinoneHCID 84497—

반응 단계

A solution of fluorenone ketyl was prepared by mixing 9 g. of fluorenone and 6.5 g. of sodium in anhydrous toluene. To this solution was added a hot solution of 37 g. of anhydrous quinidine base in 150 ml. of anhydrous toluene. After 15 minutes at reflux, the reaction was complete. After extraction and neutralization treatments as in Example I, 36 g. of pure quinidinone (TLC) was obtained (97% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04175192
출처 데이터셋uspto-grants-1979_11
ORD IDord-2e349f16a0ab4c7baaf37321e4e4dae6
출처 메모uspto-grants-1979_11