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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21312생성일: 2026년 10월 25일

Ammonium fluoride → 4-Chloro-5-(2-furyl)-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone

https://huagongshe.com/reaction/21312

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium fluorideHCID 25516—
반응물Lithium ChlorideHCID 433294—
반응물2-(Tributylstannyl)furanHCID 4393688—
반응물4-Chloro-5-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinoneHCID 86628329—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물4-Chloro-5-(2-furyl)-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinoneHCID 6848734660.1%

반응 조건

온도90 °C

반응 단계

4-Chloro-5-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone (100 mg, 0.159 mmol) was dissolved in 1,4-dioxane (3.0 mL), and the solution was added with 2-(tributylstannyl)furan (0.150 mL, 0.477 mmol), tetrakis(triphenylphosphine)palladium (15.0 mg, 0.0130 mmol) and lithium chloride (60.6 mg, 1.43 mmol), followed by stirring at 90° C. for 6.0 hours under argon atmosphere. The reaction mixture was added with 10% aqueous ammonium fluoride solution and filtered using Celite. The filtrate was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by preparative thin-layer chromatography (chloroform/methanol=6/1) to obtain 4-chloro-5-(2-furyl)-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone (52.2 mg, yield 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c6905c7eb97e4bdb8122dce196f0807e
출처 메모uspto-grants-2010_06