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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| 반응물 | tert-butyl (3R)-3-aminopiperidine-1-carboxylate | HCID 1501974 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester | HCID 59073577 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08653089B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-f0deb9b4db2e463f80f81f0487975eb6 |
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| 출처 메모 | uspto-grants-2014_02 |
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