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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11602생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/11602

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-3-nitropyridineHCID 79613—
반응물N-[tert-butoxycarbonyl]-L-serineHCID 98766—
용매DimethylformamideHCID 6228—
생성물N-t-butyloxycarbonyl-O-(3-nitro-2-pyridyl)-L-serineHCID 6919633474.5%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098235B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0855fb1c75354af99d14871d375e7943
출처 메모uspto-grants-2006_08