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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242818생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/242818

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물tert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
용매DimethylformamideHCID 6228—
생성물(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 5907357777.2%

반응 조건

온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653089B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f0deb9b4db2e463f80f81f0487975eb6
출처 메모uspto-grants-2014_02