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HRID 876248作成日:2026年10月26日

Triethylamine → 4-Nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/876248

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Nitrophenyl chloroformateHCID 82129—
反応物Sodium BicarbonateHCID 516892—
反応物N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamideHCID 66701397—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物4-Nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylateHCID 66701467—

反応条件

温度0 °C

反応手順

At 0° C., 1.5 g (4.3 mmol) of N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide and 1.2 ml (1.1 mmol) of triethylamine were initially charged in 131 ml of dichloromethane, and 868 mg (4.3 mmol) of 4-nitrophenyl chlorocarbonate were added slowly. The mixture was stirred at 0° C. for 2 h and then warmed to RT. Water and saturated aqueous sodium bicarbonate solution were added, and the reaction mixture was extracted. The organic phase was concentrated under reduced pressure and purified by column chromatography (cyclohexane/ethyl acetate 1:2). Yield: 1.95 g (88% of theory)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987248B2
出典データセットuspto-grants-2015_03
ORD IDord-5ad197d86fac4986b747e1ecf455f861
出典メモuspto-grants-2015_03