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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 373324생성일: 2026년 10월 25일

2-Methylpiperazine → rac-1-Ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinoline-carboxylic acid monosodium salt

https://huagongshe.com/reaction/373324

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylpiperazineHCID 66057—
반응물7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 483169—
반응물Sodium 2-ethylhexanoateHCID 23672331—
용매ChloroformHCID 6212—
용매Ethyl AcetateHCID 8857—
생성물rac-1-Ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinoline-carboxylic acid monosodium saltHCID 6789624775%

반응 단계

A mixture of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid [J. Med. Chem., 23, 1358 (1980)] (0.52 g, 2 mmol) and 2-methylpiperazine (0.8 g, 8 mmol) was heated at 175° for 5 hours. The residue was dissolved in ethylacetate (10 mL) and chloroform (10 mL), and a solution of sodium-2-ethyl- hexanoate (0.33 g, 2 mmol) in ethyl acetate (20 mL) was added. The mixture was stirred for 30 minutes and the precipitate was collected. The crude product was purified by preparative liquid chromatography (C-18 reverse phase, gradient 0-40% acetonitrile in water) to give a pale yellow lyophilized solid (0.5 g, 75% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162523
출처 데이터셋uspto-grants-1992_11
ORD IDord-f139f0669db54306a99a6acbf3f14bfb
출처 메모uspto-grants-1992_11