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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241986생성일: 2026년 10월 25일

Potassium Iodide → HCID 46896511, 화합물

https://huagongshe.com/reaction/241986

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물TributylphosphineHCID 13831—
반응물1-(4-(Chloromethyl)phenyl)-1H-imidazoleHCID 7063859—
반응물HCID 178514319HCID 178514319—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물HCID 46896511HCID 46896511—

반응 단계

4-Diazo-2,5-bis(2-fluorophenyl)-2,4-dihydro-3H-pyrazol-3-one (0.17 g, 0.56 mmol) was dissolved in acetonitrile (5 mL) and treated with tri-n-butylphosphine (0.11 g, 0.56 mmol, 1.0 equiv). After stirring for 30 minutes at ambient temperature, 1-[4-(chloromethyl)phenyl]-1H-imidazole (0.11 g, 0.56 mmol, 1.0 equiv), potassium iodide (47 mg, 0.28 mmol, 0.5 equiv) and potassium carbonate (97 mg, 0.70 mmol, 1.25 equiv) were added at ambient temperature. After 45 minutes, the reaction mixture was warmed to 85° C., stirred for 2.5 hours and then cooled to ambient temperature. The mixture was poured into water (100 mL), extracted with ethyl acetate (2×75 mL) and the combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified twice by silica gel gradient chromatography (100:0 to 0:100; hexanes:ethyl acetate containing 10% methanol; and then 100:0 to 90:10; dichloromethane:methanol containing 10% ammonium hydroxide), providing the titled compound as a deep red solid: 1H-NMR (400 MHz, CDCl3) δ 8.33 (1H, dd, J=7.6, 1.8 Hz), 7.85 (1H, br s), 7.67-7.53 (4H, m), 7.46 (2H, d, J=8.5 Hz), 7.40 (2H, d, J=8.5 Hz), 7.42-7.37 (1H, m), 7.31-7.20 (4H, m), 5.88 (2H, s) ppm; high resolution mass spectrometry (ES+) m/z 437.1526 [(M+H)+; calculated for C25H18FN6O: 437.1521].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653079B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7f12b7f3609f415dab3821db2a863fff
출처 메모uspto-grants-2014_02