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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25175생성일: 2026년 10월 24일

Diisopropyl Ether → 1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-7-(3-ethylaminoazetidin-1-yl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

https://huagongshe.com/ko/reaction/25175

반응식

참여 물질

역할이름HCID투입량
반응물Diisopropyl EtherHCID 7914—
반응물1-MethylpyrrolidineHCID 8454—
반응물N-ethylazetidin-3-amineHCID 10336591—
반응물1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 15486977—
용매Dimethyl SulfoxideHCID 679—
생성물1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-7-(3-ethylaminoazetidin-1-yl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 995804977.6%

반응 조건

온도40 °C

반응 단계

3-Ethylaminoazetidine (700 mg), 1-(6-amino-3,5-difluoropyridin-2-yl)-8-bromo-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (1.5 g), N-methyl-pyrrolidine (2.0 g)and dimethylsulfoxide (4.5 g) were combined, and the mixture was heated under stirring at 40° C. for 24 hours. After the mixture was allowed to cool down, isopropyl ether (10 mL) was added, the mixture was stirred, and a clear layer at the top of the mixture was removed. The same procedure was repeated once more, and the residue was concentrated under reduced pressure. Ethanol (5 mL) was added, and the mixture was heated under stirring at 70° C. for 30 minutes. The precipitated solid was collected by filtration. The title compound (1.38 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858625B1
출처 데이터셋uspto-grants-2005_02
ORD IDord-f1b6525d2c034223888dbf7e1495eaa4
출처 메모uspto-grants-2005_02