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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727870생성일: 2026년 10월 26일

Water → (4-Tert-butylcyclohexyl)-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]amine

https://huagongshe.com/reaction/1727870

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-tert-ButylcyclohexanoneHCID 7392—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(4-Tert-butylcyclohexyl)-[4-(6,7-dimethoxyquinolin-4-yloxy)phenyl]amineHCID 1011379511.4%

반응 조건

온도60 °C

반응 단계

4-(6,7-Dimethoxy-4-quinolyloxy)aniline (300 mg) was dissolved in N,N-dimethylformamide (10 ml) to prepare a solution. 4-Tert-butylcyclohexanone (200 mg) was then added to the solution, and the mixture was stirred at 60° C. for one hr. The reaction solution was cooled to room temperature before sodium triacetoxy borohydride (400 mg) was added thereto. The mixture was then stirred at room temperature for 3 hr. Water and ethyl acetate were added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and was dried over sodium sulfate. The solvent was removed by evaporation under the reduced pressure, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (50 mg, yield 11%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07495104B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-0d993d71c9dd4f9da18e2a28b9b43173
출처 메모uspto-grants-2009_02