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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1589564생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1589564

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물1-Ethyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 800521—
반응물2,5-Diazabicyclo(2.2.2)octane dihydrochlorideHCID 22924390—
용매AcetonitrileHCID 6342—
생성물7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1356579543.4%

반응 단계

A solution of 0.52 g (2.0 mmole) of 1-ethyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 0.37 g (2.0 mmole) of 2,5-diazabicyclo(2.2.2)octane dihydrochloride [P. A. Sturm et al., J. Med. Chem., 17, 481 (1974)], 0.90 ml (6.0 mmole) of 1,8-diazabicyclo[5.4.0]undec-7-ene and 25 ml of acetonitrile was heated under reflux for 21 hours. The reaction mixture was filtered and the filtrate was evaporated to dryness. The residue was recrystallized from ethanol to give 0.30 g of the title compound, mp 270°-272°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04571396
출처 데이터셋uspto-grants-1986_02
ORD IDord-9cd97c866e664a92aa9f435b7db69aaf
출처 메모uspto-grants-1986_02