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HRID 591345作成日:2026年10月26日

Sodium Carbonate → Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/591345

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物6-fluoro-2,3-dihydro-1H-indoleHCID 260400—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylateHCID 89613009—

反応手順

To a solution of 6-fluoroindoline (9.36 g, 68 mmol) in CH2Cl2 (100 mL) was added 1-Boc-4-piperidone (13.6 g, 68 mmol). The resulting mixture was stirred at room temperature for 1 h and NaBH(OAc)3 (18 g, 85 mmol, 1.25 equiv) was added. The resulting mixture was stirred at room temperature for 24 h and was then poured slowly to a vigorously stirred Na2CO3(aq). After 30 min stirring, the layers were separated. The aqueous layer was extracted with CH2Cl2 (100 mL). The combined organic layer was washed with brine (100 mL), dried (Na2SO4), and filtered. The solvent was removed by roto-evaporator, Et2O (10 mL) and then hexane (150 mL) were added to the resulting residue. The mixture was allowed to stand, resulting in the formation of a white solid, which was collected and washed with 5% Et2O/hexane and then dried. This was repeated to yield three crops of tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238658B2
出典データセットuspto-grants-2016_01
ORD IDord-b2d5a6cb376e42f7ab91332e28db0afd
出典メモuspto-grants-2016_01