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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133127생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/133127

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium BicarbonateHCID 516892—
반응물Binap, (A+-)-HCID 634876—
반응물(2,3-Difluorophenyl)boronic acidHCID 2734333—
반응물benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoateHCID 25034374—
용매1,4-DioxaneHCID 31275—
생성물benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinateHCID 25034375—

반응 단계

A solution of benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoate from Step B (34.0 g, 73.2 mmol), 2,3-difluorophenylboronic acid (28.9 g, 183 mmol) and water (4.62 mL, 256 mmol) in dioxane (240 mL) was degassed with argon for 15 min. To this solution was added sodium bicarbonate (3.08 g, 36.6 mmol), (S)-BINAP (1.28 g, 2.05 mmol) and acetylacetanotobis(ethylene)rhodium(I) (0.472 g, 1.83 mmol). The mixture was stirred at ambient temperature for 2 min then heated to 35° C. After 4 h, (S)-BINAP (255 mg, 0.41 mmol) and acetylacetanotobis(ethylene)rhodium(I) (94 mg, 0.36 mmol) were added. After an additional 2 h, the reaction was partitioned between CH2Cl2 and aqueous NaHCO3. The aqueous layer was extracted with another portion of CH2Cl2. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—95:5 to 40:60, to give the title compound. MS: m/z=379 (M-C10H15O4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390798B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-655db2625b2c42b2910333d659e0c125
출처 메모uspto-grants-2008_06