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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344845생성일: 2026년 10월 23일

Triethylamine → (RS)-7-fluoro-1-methyl-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/ko/reaction/344845

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-PhenylpiperazineHCID 250673—
반응물8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700554—
용매PyridineHCID 1049—
생성물(RS)-7-fluoro-1-methyl-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 988902535.5%

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 (1.84 g) in pyridine (20 cc), (RS)-2-phenylpiperazine (5.83 g) and triethylamine (1.24 g) is heated to a temperature in the region of 115° C. for 5 hours. After cooling to approximately 20° C., the precipitate formed is drained and washed with pyridine (2×5 cc), isopropyl alcohol (2×5 cc), ethanol (2×5 cc) and ethyl ether (1×20 cc). After 1 recrystallization in a mixture of dimethylformamide (40 cc) and ethanol (40 cc), (RS)-7-fluoro-1-methyl-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (0.920 g) is obtained in the form of a yellow solid, m.p. 265° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053509
출처 데이터셋uspto-grants-1991_10
ORD IDord-da4a0a6f37b1432da53cb69c5b8b0d02
출처 메모uspto-grants-1991_10