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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254868생성일: 2026년 10월 26일

Acetonitrile → Gatifloxacin

https://huagongshe.com/reaction/254868

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물2-Methylpiperazine dihydrochlorideHCID 517620—
반응물1-Cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acidHCID 7019465—
용매TriethylamineHCID 8471—
생성물GatifloxacinHCID 537993.1%

반응 단계

An acetonitrile solution (30 mL) containing 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid (3 g), 2-methylpiperazine dihydrochloride (1.93 g), triethylamine (1.43 mL), and boron trifluoride-tetrahydrofuran complex (2.84 g) was stirred at room temperature for one hour. Triethylamine (5.71 mL) was further added to the reaction mixture, followed by stirring at room temperature for 24 hours. The solvent was evaporated under reduced pressure, and methanol (30 mL) was added to the residue. The mixture was refluxed for 5 hours, and the solvent was evaporated under reduced pressure. 80% Hydrated methanol (30 mL) was added to the residue, and the pH of the product was adjusted to 7 by use of 5N aqueous sodium hydroxide solution, followed by stirring at room temperature for 16 hours. The thus-produced crystals were recovered through filtration and dried, to thereby yield 3.55 g of the title compound (yield: 91%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875722B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-5abf108034464d119527a4dc3e0328a7
출처 메모uspto-grants-2011_01