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HRID 14390作成日:2026年10月26日

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

https://huagongshe.com/reaction/14390

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium BicarbonateHCID 516892—
反応物(2,3-Difluorophenyl)boronic acidHCID 2734333—
反応物benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoateHCID 25034374—
触媒Binap, (A+-)-HCID 634876—
溶媒1,4-DioxaneHCID 31275—
溶媒Sodium bicarbonate methylene chlorideHCID 23716255—
生成物benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinateHCID 2503437587.4%

反応手順

A solution of benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoate (34.0 g, 73.2 mmol), 2,3-difluorophenylboronic acid (28.9 g, 183.0 mmol) and water (4.62 mL, 256.2 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 RT for 2 min then heated to 35° C. After 4 h, 255 mg of (S)-BINAP and 94 mg of acetylacetanotobis(ethylene)rhodium(I) were added. After an additional 2 h the reaction was diluted with DCM/NaHCO3, the layers separated and the aqueous phase was backwashed with another portion of DCM. The combined organics were dried over magnesium sulfate, filtered and concentrated to give a residue that was purified by silica gel chromatography (5%→60% ethyl acetate/hexanes) to give the title compound (37.0 g, 87%) contaminated with ˜5% 5R isomer. MS 379.1 (M+1−Boc).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732438B2
出典データセットuspto-grants-2010_06
ORD IDord-1bdf3ad0aecb4fffad466c9a8fc1e468
出典メモuspto-grants-2010_06