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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1870614생성일: 2026년 10월 25일

1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidine → 4-(2-Amino-4-fluoro-phenylamino)-piperidine-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1870614

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidineHCID 13792162—
촉매PlatinumHCID 23939—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Amino-4-fluoro-phenylamino)-piperidine-1-carboxylic acid ethyl esterHCID 13792172—

반응 단계

This 1-ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidine (5.7 g, 18.3 mmol.) was dissolved in THF (50 mL) and diluted with ethanol (100 mL). After addition of 5% platinum/carbon catalyst (1.2 g), the hydrogenation of the nitro functional group was carried out at atmospheric pressure via a balloon over a four hour period. The catalyst was removed and the solvents evaporated to give 1-ethoxycarbonyl-4-(2-amino-4-fluoroanilino)-piperidine as a viscous oil which was used as is.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06096763
출처 데이터셋uspto-grants-2000_08
ORD IDord-9183a7014d3848bc85fc967bbbeff005
출처 메모uspto-grants-2000_08