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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111448생성일: 2026년 10월 24일

1-Methylpiperazine → 1-Cyclopropyl-6-fluoro-8-methoxy-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/ko/reaction/1111448

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물1-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acidHCID 7019465—
용매Dimethyl SulfoxideHCID 679—
생성물1-Cyclopropyl-6-fluoro-8-methoxy-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 1073823219.7%

반응 단계

A mixture of 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid (200 mg), N-methylpiperazine (140 mg) and anhydrous DMSO (3 ml) was stirred for 5 hours at 70° to 95° C. on an oil bath. The reacting mixture was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography eluting with chloroform-methanol-concentrated aqueous ammonia (20:6:1), the residue was recrystallized from methanol to give the title compound (50 mg) as colorless needles, mp 221°-222° C. (decompd.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04980470
출처 데이터셋uspto-grants-1990_12
ORD IDord-9a50f3078fcf4a9e88eda4a7bed14d60
출처 메모uspto-grants-1990_12