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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1292생성일: 2026년 10월 24일

Ethanol → 7-(1-Piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/ko/reaction/1292

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium HydroxideHCID 14798—
반응물Ethyl 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylateHCID 15345961—
용매WaterHCID 962—
생성물7-(1-Piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 1465116656.4%

반응 단계

To ethyl 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate (23 mg) are added 10% aqueous solution of sodium hydroxide (3 ml) and ethanol (3 ml), and the mixture is refluxed for 1 hour. After cooling, the reaction mixture is diluted with water and washed with dichloromethane. After the aqueous layer is made acidic with acetic acid and then made weak alkaline with an aqueous sodium hydrogen carbonate. The resultant is extracted with dichloromethane and the extract is dried. The solvent is distilled off under reduced pressure and to the residue is added ethanol. The precipitated crystals are filtered and recrystallized from dimethylformamide to give 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (12 mg), as white powder, m.p. 231°-233° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723648
출처 데이터셋uspto-grants-1998_03
ORD IDord-cf9ee368bd9548f6bc7d6beba130ae9b
출처 메모uspto-grants-1998_03