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HRID 45583作成日:2026年10月25日

tert-Butyl 4-oxopiperidine-1-carboxylate → 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/45583

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物5-FluoroindolineHCID 2774463—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Sodium bicarbonate waterHCID 86585896—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indoleHCID 67417842—

反応手順

To a solution of 5-fluoroindoline (1.0 g, 7.30 mmol) and N-Boc-4-piperidone (1.60 g, 7.50 mmol) in tetrahydrofuran (10.0 mL) was added sodium triacetoxyborohydride (1.80 g, 7.50 mmol). After stirring for 3 hours at room temperature, to the mixture were added saturated sodium bicarbonate water and ethyl acetate, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified with silica gel column (chloroform/methanol=98/2 to 90/10) to give a Boc derivative of the title compound. MS (ESI+) 321 (M++1, 100%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541585B2
出典データセットuspto-grants-2013_09
ORD IDord-e200522c45314eee9bac792acc4c12d9
出典メモuspto-grants-2013_09