돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31145생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/31145

반응식

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 번호US07425550B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-29042cdc7dcd480dae656ad35e772398
출처 메모uspto-grants-2008_09