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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1254465생성일: 2026년 10월 26일

2-Methyltetrahydrofuran → (E)-4-(2-(2-chloro-4-fluorophenyl)-1-(1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)but-1-en-1-yl)benzaldehyde

https://huagongshe.com/reaction/1254465

반응식

참여 물질

역할이름HCID투입량
반응물2-MethyltetrahydrofuranHCID 7301—
반응물Cesium carbonateHCID 10796—
반응물Potassium HydroxideHCID 14797—
반응물4-IodobenzaldehydeHCID 96657—
반응물Bis(pinacolato)diboraneHCID 2733548—
반응물2-Chloro-4-fluoro-1-iodobenzeneHCID 2736559—
반응물5-(But-1-yn-1-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazoleHCID 66793270—
촉매HCID 178418476HCID 178418476—
촉매HCID 178420539HCID 178420539—
용매WaterHCID 962—
생성물(E)-4-(2-(2-chloro-4-fluorophenyl)-1-(1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)but-1-en-1-yl)benzaldehydeHCID 8666336985.7%

반응 조건

온도95 °C

반응 단계

A round-bottom flask equipped with a magnetic stir bar, a reflux condenser, internal thermometer, and a N2 inlet was charged with 5-(but-1-yn-1-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (50.0 g, 197 mmol; Intermediate 3), bis(pinacolato)diboron (50.4 g, 199 mmol), and anhydrous 2-methyltetrahydrofuran (393 mL) followed by Pt(PPh3)4 (1.83 g, 1.5 mmol). This mixture was degassed with three vacuum/N2 cycles, heated at 83° C. (internal temperature; oil bath at 95° C.) for 5 h under N2, and then allowed to cool to room temperature. 2-Methyltetrahydrofuran (393 mL), cesium carbonate (128.1 g, 393 mmol), and water (11.8 mL, 1.5% v/v) were added, and the reaction was cooled to 4° C. 4-Iodobenzaldehyde (45.6 g, 197 mmol) and PdCl2(PPh3)2 (6.90 g, 9.8 mmol) were added, and the reaction was degassed with three vacuum/N2 cycles. The mixture was allowed to warm to room temperature and stirred overnight. Aqueous KOH solution (4M, 275 mL, 1100 mmol) and 2-chloro-4-fluoroiodobenzene (70.6 g, 275 mmol) were added. The reaction was degassed with 3 vacuum/N2 cycles, heated at 75° C. (internal temperature; oil bath at 90° C.) for 7 h under N2, and then allowed to cool to room temperature. The layers were separated, and the organic layer was washed with brine (800 mL), dried over sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (0-20% ethyl acetate in hexanes) to give the title compound (82.6 g, 7:1 mixture of regioisomers) as a pale yellow foam. Data for major isomer; (E)-4-(2-(2-chloro-4-fluorophenyl)-1-(1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl)but-1-en-1-yl)benzaldehyde: 1H NMR (300 MHz, DMSO-d6): δ 9.82 (s, 1H), 8.15 (s, 1H), 7.78-7.71 (m, 2H), 7.61 (d, 2H), 7.43-7.27 (m, 3H), 7.15 (m, 3H), 5.86 (dd, 1H), 3.93-3.85 (m, 1H), 3.79-3.68 (m, 1H), 2.44-2.36 (m, 3H), 2.10-1.96 (m, 2H), 1.81-1.67 (m, 1H), 1.63-1.53 (m, 2H), 0.92 (t, 3H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08455534B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-cdea740ebefa4b72b172ab68d66c662b
출처 메모uspto-grants-2013_06