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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228944생성일: 2026년 10월 24일

Water → 3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6-dimethyl-[2,3']bipyridine

https://huagongshe.com/ko/reaction/228944

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
반응물5,6-Dimethyl-3-hydroxy-[2,3']bipyridineHCID 23156516—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매1,2-DichlorobenzeneHCID 7239—
생성물3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6-dimethyl-[2,3']bipyridineHCID 5775657188%

반응 조건

온도140 °C

반응 단계

5,6-Dimethyl-3-hydroxy-[2,3′]bipyridine (400 mg), 7-benzyloxy-4-chloro-6-methoxyquinoline (1.80 g), and 4-dimethylaminopyridine (732 mg) were suspended in o-dichlorobenzene (8 ml), and the suspension was stirred at 140° C. for 6 hr. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was 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 column chromatography using chloroform-methanol to give the title compound (811 mg, yield 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-3e25a30de33343f69056d7bdd3a84c10
출처 메모uspto-grants-2009_07