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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228729생성일: 2026년 10월 24일

Triethylamine → 1-[2-(6,7-Dimethoxy-quinolin-4-yloxy)-4,5-dimethyl-phenyl]-ethanone oxime

https://huagongshe.com/ko/reaction/228729

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물1-(2-((6,7-Dimethoxyquinolin-4-yl)oxy)-4,5-dimethylphenyl)ethan-1-oneHCID 10066538—
용매EthanolHCID 702—
생성물1-[2-(6,7-Dimethoxy-quinolin-4-yloxy)-4,5-dimethyl-phenyl]-ethanone oximeHCID 8660518732%

반응 단계

1-[2-(6,7-Dimethoxy-quinolin-4-yloxy)-4,5-dimethylphenyl]-1-ethanone (compound 38) (30 mg) was dissolved in ethanol (1 ml) to prepare a solution. Hydroxylamine hydrochloride (12 mg) and triethylamine (27 mg) were added to the solution, and the mixture was stirred at room temperature overnight. Further, hydroxylamine hydrochloride (12 mg) and triethylamine (27 mg) were then added to the reaction solution, and the mixture was stirred at room temperature for 5 hr. The solvent was removed by distillation under the reduced pressure, water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water 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 hexane-acetone to give the title compound (10 mg, yield 31%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-b15d0aed05834478b77655be55040419
출처 메모uspto-grants-2009_07