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HRID 21000作成日:2026年10月26日

Acetic Acid → 3-Amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimide

https://huagongshe.com/reaction/21000

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1-(2-Hydroxyethyl)piperazineHCID 7677—
反応物Sodium CarbonateHCID 10340—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-Amino-6-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]phthalimideHCID 86628226—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物3-Amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimideHCID 6849203738.5%

反応手順

3-Amino-6-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]phthalimide (45.0 mg, 0.111 mmol) was dissolved in acetonitrile (2 mL), and the solution was added with 1-(2-hydroxyethyl)piperazine (57 mg, 0.440 mmol), acetic acid (0.508 mL, 8.87 mmol) and sodium triacetoxyborohydride (118 mg, 0.557 mmol), followed by stirring at room temperature for 2.5 hours. The reaction mixture was added with water and sodium carbonate, 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 flash column chromatography (hexane/ethyl acetate=4/1, 1/1) to obtain 3-amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimide (22.2 mg, yield 38%).

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-0a946f786c784e549ef91a1a15cd543b
出典メモuspto-grants-2010_06