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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2291275생성일: 2026년 10월 26일

2-Methylpiperazine → 3-Quinolinecarboxylic acid, 1,4-dihydro-5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-4-oxo-

https://huagongshe.com/reaction/2291275

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylpiperazineHCID 66057—
반응물5-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 13910947—
용매PyridineHCID 1049—
생성물3-Quinolinecarboxylic acid, 1,4-dihydro-5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-4-oxo-HCID 306668488.3%

반응 단계

A mixture of 5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.25 g), 2-methylpiperazine (2.0 g), and pyridine (13 ml) was heated at 105°-110° C. for 1 hour with stirring. The reaction mixture was evaporated to dryness under reduced pressure and water was added to the residue. The mixture was extracted with chloroform and the extract was dried. After evaporation of chloroform, ethanol was added to the residue. The resulting crystals were filtered and recrystallized from chloroform-ethanol to give 5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.4 g), m.p. 251°-253° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04795751
출처 데이터셋uspto-grants-1989_01
ORD IDord-7575f8ad516d41479d5f0b19a63d9fe6
출처 메모uspto-grants-1989_01