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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228752생성일: 2026년 10월 24일

Water → [3-(6,7-Dimethoxy-quinolin-4-yloxy)-6-methyl-pyridin-2-yl]-(6-methyl-pyridin-2-yl)-methanol

https://huagongshe.com/ko/reaction/228752

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물6-Methyl-2-pyridinecarboxaldehydeHCID 70737—
반응물4-[(2-Iodo-6-methyl-3-pyridyl)oxy]-6,7-dimethoxyquinolineHCID 10093673—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물[3-(6,7-Dimethoxy-quinolin-4-yloxy)-6-methyl-pyridin-2-yl]-(6-methyl-pyridin-2-yl)-methanolHCID 2307828873.8%

반응 조건

온도-78 °C

반응 단계

4-(2-Iodo-6-methyl-pyridin-3-yloxy)-6,7-dimethoxyquinoline (compound 116) (100 mg) was dissolved in tetrahydrofuran (7 ml) to prepare a solution which was then brought to −78° C. n-Butyllithium hexane solution (0.22 ml) was slowly added dropwise thereto, and the mixture was stirred at −78° C. for 20 min. 6-Methyl-2-pyridine-carbaldehyde (57 mg) was dissolved in tetrahydrofuran (7 ml) to prepare a solution which was then added dropwise to the reaction solution, followed by stirring at room temperature for 5 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-acetone to give [3-(6,7-dimethoxy-quinolin-4-yloxy)-6-methyl-pyridin-2-yl]-(6-methyl-pyridin-2-yl)-methanol (73 mg, yield 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-0d51150efd0946e6bcbbdc7952f139f4
출처 메모uspto-grants-2009_07