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HRID 21107作成日:2026年10月26日

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

https://huagongshe.com/reaction/21107

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Butyn-1-OLHCID 13566—
反応物3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimideHCID 68488747—
触媒Copper iodideHCID 83717—
触媒HCID 178418476HCID 178418476—
溶媒DiethylamineHCID 8021—
生成物3-Amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimideHCID 6849277887%

反応条件

温度50 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745641B2
出典データセットuspto-grants-2010_06
ORD IDord-5cb5ea9590ec49be94d9bad2c5ae3039
出典メモuspto-grants-2010_06