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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1467703생성일: 2026년 10월 26일

Ethanol → Ethyl 2-(4-fluorophenyl)-3-(1-methyl-1H-imidazo[4,5-c]pyridin-2-yl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate

https://huagongshe.com/reaction/1467703

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1-Methyl-1H-imidazo(4,5-c)pyridine-2-carboxaldehydeHCID 12239331—
반응물HCID 178519076HCID 178519076—
용매Ethyl PropionateHCID 7749—
생성물Ethyl 2-(4-fluorophenyl)-3-(1-methyl-1H-imidazo[4,5-c]pyridin-2-yl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylateHCID 6726193714%

반응 단계

To a solution of 1-methyl-1H-imidazo[4,5-c]pyridine-2-carbaldehyde (400 mg, 2.48 mmol), (E)-4-(4-fluorobenzylideneamino) isobenzofuran-1(3H)-one (634 mg, 2.48 mmol) in ethyl propionate (20 ml) were added a solution of sodium ethanoxide in ethanol [sodium (171 mg, 7.45 mmol) in ethanol (10 mL)] at 0° C. Then the mixture was stirred at room temperature overnight. Then the mixture was quenched with water (10 mL) and solvent was removed in vacuum. The residue was extracted with ethyl acetate (100 mL×4). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude product, which was purified by chromatography (silica gel, petroleum ether/ethyl acetate=25:1 to 5:1) to give the title compound (150 mg, yield 14%). LC-MS (ESI) m/z: 445 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08999987B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-4f724727a436447284d3d96abdebd152
출처 메모uspto-grants-2015_04