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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229068생성일: 2026년 10월 25일

Methanesulfonic Acid → 6-Methoxy-4-(5,6,6'-trimethyl-[2,2']bipyridin-3-yloxy)-quinolin-7-ol

https://huagongshe.com/reaction/229068

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참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6,6'-trimethyl-[2,2']bipyridineHCID 57756540—
용매Trifluoroacetic acidHCID 6422—
생성물6-Methoxy-4-(5,6,6'-trimethyl-[2,2']bipyridin-3-yloxy)-quinolin-7-olHCID 136131624112.4%

반응 조건

온도70 °C

반응 단계

3-(7-Benzyloxy-6-methoxy-quinolin-4-yloxy)-5,6,6′-trimethyl-[2,2′]bipyridine (compound 442) (475 mg) was dissolved in trifluoroacetic acid (4.7 ml) to prepare a solution. Methanesulfonic acid (0.47 ml) was added to the solution, and the mixture was stirred at 70° C. for one hr. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. An aqueous sodium hydrogencarbonate solution was then added to the residue, 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 (433 mg, yield 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-4f1c58b8c7a14ae98d162f9daf01ad75
출처 메모uspto-grants-2009_07