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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344861생성일: 2026년 10월 26일

Acetic Acid → (RS)-7-Fluoro-1-methoxy-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/344861

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물2-PhenylpiperazineHCID 250673—
반응물7,8-Difluoro-1-methoxy-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14853343—
용매Dimethyl SulfoxideHCID 679—
생성물(RS)-7-Fluoro-1-methoxy-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 5371203568.3%

반응 조건

온도20 °C

반응 단계

A suspension of 7,8-difluoro-1-methoxy-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (2 g) and (RS)-2-phenylpiperazine (2.1 g) in dimethyl sulphoxide (30 cc) is heated with stirring for 15 minutes to approximately 50° C. After cooling to approximately 20° C., the reaction mixture is poured into water (100 cc) and treated with acetic acid (1.2 cc). The insoluble matter is drained, washed with water (3×10 cc) and recrystallized in dimethylformamide (80 cc). (RS)-7-Fluoro-1-methoxy-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (2 g) is obtained in the form of a yellow solid, decomposing at 284° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053509
출처 데이터셋uspto-grants-1991_10
ORD IDord-cfbe001748004234ba70b60613066247
출처 메모uspto-grants-1991_10