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HRID 20982作成日:2026年10月24日

Acetic Acid → tert-butyl 4-(1H-indol-5-ylamino)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/20982

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5-AminoindoleHCID 78867—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物tert-butyl 4-(1H-indol-5-ylamino)piperidine-1-carboxylateHCID 66650318125.6%

反応手順

5-Aminoindole (100 mg, 0.757 mmol) was dissolved in acetonitrile (2 mL), and the solution was added with 1-(tert-butoxycarbonyl)-4-piperidinone (181 mg, 0.908 mmol), acetic acid (0.870 mL, 15.2 mmol) and sodium triacetoxyborohydride (160 mg, 0.755 mmol) little by little, followed by stirring at room temperature for 1 hour. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 5-[1-(tert-butoxycarbonyl)-4-piperidylamino]indole (300 mg).

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-7553ba8747dd4129bdae1918f61fc2ba
出典メモuspto-grants-2010_06