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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21107생성일: 2026년 10월 25일

Water → 3-Amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide

https://huagongshe.com/reaction/21107

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Butyn-1-OLHCID 13566—
반응물3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimideHCID 68488747—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매DiethylamineHCID 8021—
생성물3-Amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimideHCID 6849277887%

반응 조건

온도50 °C

반응 단계

3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide (150 mg, 0.298 mmol) was dissolved in diethylamine (7.5 mL), and the solution was added with bis(triphenylphosphine)dichloropalladium (16.7 mg, 0.0234 mmol), copper iodide (11.4 mg, 0.0596 mmol) and 3-butyn-1-ol (0.226 mL, 2.98 mmol), followed by stirring at 50° C. for 3.7 hours under argon atmosphere. The reaction mixture was added with water and 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=10/1) to obtain 3-amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide (115 mg, yield 87%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5cb5ea9590ec49be94d9bad2c5ae3039
출처 메모uspto-grants-2010_06