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HRID 501132作成日:2026年10月27日

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

https://huagongshe.com/reaction/501132

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+1-2Boc).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772224B2
出典データセットuspto-grants-2010_08
ORD IDord-e4c6aaf95b64446b98c6b23410e8d15e
出典メモuspto-grants-2010_08