돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245189생성일: 2026년 10월 26일

2-Oxobutanoic Acid → 6-Fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

https://huagongshe.com/reaction/245189

반응식

참여 물질

역할이름HCID투입량
반응물2-Oxobutanoic AcidHCID 58—
반응물3-(Trifluoromethyl)benzaldehydeHCID 67990—
반응물4-Fluoro-3-methoxyanilineHCID 2774533—
용매EthanolHCID 702—
생성물6-Fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acidHCID 6738400249.2%

반응 단계

A solution of 4-fluoro-3-(methyloxy)aniline (13.6 g, 96 mmol) and 3-(trifluoromethyl)benzaldehyde (16.78 g, 96 mmol) in ethanol (200 mL) was heated to reflux for 1 h. 2-Oxobutanoic acid (9.84 g, 96 mmol) was added portionwise. The reaction mixture was stirred at reflux for an additional 3 h, cooled to room temperature, and stirred overnight. The solid was collected by filtration, washed with ethanol, and air dried to afford 6-fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (17.9 g, 49% yield). 1H NMR (400 MHz, DMSO-d6)™ 14.34 (br. s., 1H), 7.93-7.98 (m, 2H), 7.88 (d, J=7.78 Hz, 1H), 7.77 (t, J=7.65 Hz, 1H), 7.71 (d, J=8.53 Hz, 1H), 7.54 (d, J=12.05 Hz, 1H), 4.03 (s, 3H), 2.38 (s, 3H); MS (m/z) 380.1 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658636B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-c3737da9472248bc8d7a7fb69787410b
출처 메모uspto-grants-2014_02