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HRID 242818作成日:2026年10月27日

Potassium Carbonate → (R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester

https://huagongshe.com/reaction/242818

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
反応物tert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
溶媒DimethylformamideHCID 6228—
生成物(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 5907357777.2%

反応条件

温度120 °C

反応手順

A mixture of 1-fluoro-2-nitrobenzene (1.41 g, 10.0 mmol), (R)-3-aminopiperidine-1-carboxylic acid tertbutyl ester (2 g, 10.0 mmol) and potassium carbonate (152 mg, 11.0 mmol) in DMF (18 mL) was heated to 120° C. under microwave irradiation for 30 min. The reaction mixture was partitioned between EtOAc (150 mL) and water. The organic layer was washed with brine, dried (Na2SO4) and then concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, eluant 10% EtOAc in DCM) affording (R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester as an orange oil (2.48 g, 77%). LCMS: RT 3.95 min [M+H-tBu]+ 266.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-f0deb9b4db2e463f80f81f0487975eb6
出典メモuspto-grants-2014_02