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HRID 31145作成日:2026年10月25日

Water → N-t-butyloxycarbonyl-O-(3-nitro-2-pyridyl)-L-serine

https://huagongshe.com/reaction/31145

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 hydrideHCID 24758—
反応物2-Chloro-3-nitropyridineHCID 79613—
反応物N-[tert-butoxycarbonyl]-L-serineHCID 98766—
溶媒DimethylformamideHCID 6228—
生成物N-t-butyloxycarbonyl-O-(3-nitro-2-pyridyl)-L-serineHCID 6919633474.5%

反応条件

温度0 °C

反応手順

To a stirring solution of N-t-butyloxycarbonyl-L-serine (2.26 g) in N,N-dimethylformamide (15 mL) under argon at −20° C. was slowly added sodium hydride (60% oil dispersion, 0.88 g gross weight). The resulting mixture was warmed to 0° C. for 1 h, then recooled to −20° C. before a solution of 2-chloro-3-nitropyridine (1.6 g) in N,N-dimethylformamide (10 mL) was added over 10 min. The resulting red solution was stirred at −20° C. for 1 h. Water (100 mL) was then added, and the mixture was washed with diethyl ether (30 mL twice). The aqueous layer was adjusted to pH 7 with 1.0 M aqueous hydrochloric acid and extracted with ethyl acetate (30 mL three times). The combined extracts were washed with brine (50 mL), dried over anhydrous sodium sulfate, and evaporated under vacuum. The resulting residue was purified by silica gel chromatography eluting with ethyl acetate-hexane (1:2) to obtain N-t-butyloxycarbonyl-O-(3-nitro-2-pyridyl)-L-serine (2.46 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425550B2
出典データセットuspto-grants-2008_09
ORD IDord-29042cdc7dcd480dae656ad35e772398
出典メモuspto-grants-2008_09