돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228582생성일: 2026년 10월 26일

Water → {2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}(5-isoxazolyl)methanone

https://huagongshe.com/reaction/228582

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Isoxazole-5-carbonyl chlorideHCID 2736707—
반응물4-(2-Bromo-4-methylphenoxy)-6,7-dimethoxyquinolineHCID 23078362—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}(5-isoxazolyl)methanoneHCID 2487910026%

반응 조건

온도-78 °C

반응 단계

4-(2-Bromo-4-methylphenoxy)-6,7-dimethoxyquinoline (100 mg) was dissolved in tetrahydrofuran (6 ml) to prepare a solution which was then cooled to −78° C. A 1.59 M n-butyllithium/hexane solution (0.4 ml) was added to the solution, and the mixture was stirred at −78° C. for 20 min. Isoxazole-5-carbonyl chloride (0.2 ml) was added to the reaction solution, and the mixture was stirred at room temperature overnight. Further, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using acetone-chloroform to give the title compound (27 mg, yield 26%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-25a0a83dff7e4caa846058ecd1d22579
출처 메모uspto-grants-2009_07