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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358860생성일: 2026년 10월 26일

Diethyl Ether → PD 135042

https://huagongshe.com/reaction/358860

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물PiperazineHCID 4837—
반응물Difluoroborane 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylateHCID 86585298—
용매Dimethyl SulfoxideHCID 679—
생성물PD 135042HCID 46556260.5%

반응 단계

0.11 g (0.00032 mole) of 1-cyclopropyl-6,7-difluoro-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate (IV) (prepared as described in Preparation 7) was dissolved in 0.5 ml of dimethyl sulfoxide, and 0.11 g (0.0012 mole) of anhydrous piperazine was added to the resulting solution. The mixture was then allowed to stand at room temperature overnight, after which it was poured into 50 ml of diethyl ether. The yellow crystals which precipitated were collected by filtration and dissolved in 30 ml of 80% aqueous ethanol and 5 ml of triethylamine, and the resulting solution was heated under reflux for 4 hours. The reaction mixture was then filtered while hot to remove insoluble material, and the filtrate was concentrated by evaporation under reduced pressure to give a crystalline substance, which was washed with ethanol to afford 0.07 g of 1-cyclopropyl-6-fluoro-8-methoxy-7-(1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as colorless powdery crystals, melting at 177°-178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04997943
출처 데이터셋uspto-grants-1991_03
ORD IDord-9fea01a665bb4c21ad93924085579c09
출처 메모uspto-grants-1991_03