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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229025생성일: 2026년 10월 27일

4-Chloro-6,7-dimethoxyquinoline → 2-(6,7-Dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoic acid

https://huagongshe.com/reaction/229025

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-6,7-dimethoxyquinolineHCID 459610—
반응물5-Fluoro-2-mercaptobenzoic acidHCID 2783371—
용매AcetonitrileHCID 6342—
생성물2-(6,7-Dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoic acidHCID 2307837731.5%

반응 단계

5-Fluoro-2-mercaptobenzoic acid (278 mg) and 4-chloro-6,7-dimethoxyquinoline (300 mg) were suspended in acetonitrile (6 ml), and the suspension was stirred at room temperature overnight. The solvent was removed by distillation under the reduced pressure. Water was added to the residue, the mixture was neutralized with sodium hydrogencarbonate and was then extracted with chloroform. The chloroform layer was washed with water and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform-methanol to give 2-(6,7-dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoic acid (152 mg, yield 31%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-a4a7f85be8454dc59ed6a9c1a3eeba17
출처 메모uspto-grants-2009_07