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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232875생성일: 2026년 10월 26일

2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepine → 2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-hydroxy-6,11-dihydrodibenz[b,e]oxepine

https://huagongshe.com/reaction/232875

반응식

참여 물질

역할이름HCID투입량
반응물2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepineHCID 23359142—
반응물HCID 178418435HCID 178418435—
용매MethanolHCID 887—
생성물2-(7-Chloro-6-fluoroquinolin-2-yl)methoxy-11-hydroxy-6,11-dihydrodibenz[b,e]oxepineHCID 2335913472.1%

반응 단계

0.5 g of sodium boron hydride was added to 2.58 g of 2-(7-chloro-6-fluoroquinolin-2-yl)methoxy-11-oxo-6,11-dihydrodibenz[b,e]oxepine obtained in Reference example 34 suspended in 70 ml of methanol and the mixture was stirred at room temperature for 11 hours. During stirring, 0.35 g of sodium boron hydride was added to the mixture twice. After completion of the reaction, the solvent was removed under reduced pressure, ice water was added to the residue and the mixture was extracted with methylene chloride. Then, the organic layer was washed with water and then dried over anhydrous sodium sulfate and the solvent was removed. The resulting solid was washed with a methylene chloride-hexane mixed solution to obtain 1.87 g of the title compound. Mass (CI); m/z=422 (M+ +1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591752
출처 데이터셋uspto-grants-1997_01
ORD IDord-de0b38d424da4514b19f65882da930be
출처 메모uspto-grants-1997_01