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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133128생성일: 2026년 10월 26일

benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinate → (5S)-N2,N2-Bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysine

https://huagongshe.com/reaction/133128

반응식

참여 물질

역할이름HCID투입량
반응물benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinateHCID 25034375—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물(5S)-N2,N2-Bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-D-lysineHCID 67526479—

반응 단계

A mixture of benzyl (5S)—N2,N2-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinate from Step C (15.5 g, 26.8 mmol) and 10% Pd/C (12.0 g) in EtOH (175 mL), was hydrogenated at 55 psi for 18 h. An additional portion of 10% Pd/C (4.0 g) was added and the reaction mixture was hydrogenated at 55 psi for a further 18 h. The reaction mixture was filtered through Celite, washing with EtOH, and the filtrate was concentrated in vacuo to afford the title compound. MS: m/z=459 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390798B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-511bfca82ab94a3c96737d18975c786b
출처 메모uspto-grants-2008_06