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HRID 20975作成日:2026年10月25日

Acetic Acid → 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole

https://huagongshe.com/reaction/20975

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Sodium CarbonateHCID 10340—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Indole-5-carboxaldehydeHCID 589040—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indoleHCID 6848993447%

反応手順

5-Formylindole (500 mg, 3.44 mmol) was dissolved in acetonitrile (10 mL), and the solution was added with 1-(tert-butoxycarbonyl)piperazine (961 mg, 5.16 mmol), acetic acid (3.90 mL, 68.1 mmol) and sodium triacetoxyborohydride (3.65 g, 17.2 mmol) little by little, followed by stirring at room temperature for 2 hours. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9, followed by extracting 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=19/1, 7/3, 1/1) to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole (505 mg, yield 47%).

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-40825bde11ad4d73a783930ebca6be83
出典メモuspto-grants-2010_06