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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344853생성일: 2026년 10월 24일

Acetic Acid → HCID 53724661, 화합물

https://huagongshe.com/ko/reaction/344853

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물2-(4-Fluorophenyl)piperazineHCID 4617623—
반응물8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700554—
용매PyridineHCID 1049—
생성물HCID 53724661HCID 5372466146.8%

반응 조건

온도115 °C

반응 단계

A suspension of 8-chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (1.6 g) and (RS)-2-(4-fluorophenyl)piperazine (3.7 g) in pyridine (16 cc) is heated to a temperature in the region of 115° C. for 24 hours. The reaction mixture is concentrated under reduced pressure (20 kPa) at approximately 60° C. The residue is taken up with ethanol (40 cc) and concentrated again under reduced pressure under the above conditions. The solid obtained is taken up with water (10 cc), treated with 10% strength acetic acid (1.75 cc), drained and washed with water (2×10 cc) and ethanol (2×10 cc). After 2 recrystallizations in dimethylformamide (10 cc each time), (RS)-7-fluoro-8-[3-(4-fluorophenyl)-1-piperazinyl]-1-methyl-4-oxo-1,4-dihydrobenzo[b ][1,8]naphthyridine-3-carboxylic acid (1.1 g) is obtained in the form of a yellow solid, m.p. 270°-275° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053509
출처 데이터셋uspto-grants-1991_10
ORD IDord-86f51b4aa94f4fa0959685c631bcb861
출처 메모uspto-grants-1991_10