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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341048생성일: 2026년 10월 26일

Potassium Carbonate → 2-(2-fluorophenyl)-5-(1H-indol-5-ylmethyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one

https://huagongshe.com/reaction/341048

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(1H-indol-5-yl)methanamineHCID 54791—
반응물(4Z)-4-[(ethoxy)methylidene]-2,5-bis(2-fluorophenyl)-2,4-dihydro-3H-pyrazol-3-oneHCID 68153972—
용매WaterHCID 962—
생성물2-(2-fluorophenyl)-5-(1H-indol-5-ylmethyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-oneHCID 52914603—

반응 단계

(4Z)-4-[(Ethoxy)methylidene]-2,5-bis(2-fluorophenyl)-2,4-dihydro-3H-pyrazol-3-one (236 mg, 0.720 mmol), potassium carbonate (100 mg, 0.720 mmol, 1 equiv) and 1-(1H-indol-5-yl)methanamine (105 mg, 0.720 mmol, 1 equiv) were combined and placed into a preheated oil bath at 100° C. open to the air for 2.5 hours. The mixture was cooled to ambient temperature, poured into water (50 mL) and extracted with ethyl acetate (3×100 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel gradient chromatography (100:0 to 90:10; dichloromethane:methanol), providing the titled compound: 1H-NMR (500 MHz, d6-DMSO) δ 11.14 (1H, s), 9.12 (1H, s), 8.18 (1H, d, J=8.0 Hz), 7.89 (1H, d, J=9.0 Hz), 7.62-7.58 (2H, m), 7.53 (1H, s), 7.51 (1H, t, J=7.7 Hz), 7.48-7.38 (3H, m), 7.36-7.32 (2H, m), 7.09 (1H, d, J=8.6 Hz), 6.40 (1H, br m), 5.78 (2H, m) ppm; low resolution mass spectrometry (ES+) m/z 409.1449 [(M+H)+; calculated for C25H18FN4O: 409.1459].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895580B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f5b4535ca4024d399f92b3f048e150fd
출처 메모uspto-grants-2014_11