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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963771생성일: 2026년 10월 24일

Pyridine → 5'-O-(2-(2-chloro-6-nitrophenyl)ethoxycarbonyl)-N4-(2-(4-nitrophenyl)ethoxycarbonyl)-2'-deoxycytidine

https://huagongshe.com/ko/reaction/963771

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2'-Deoxy-N-{[2-(4-nitrophenyl)ethoxy]carbonyl}cytidineHCID 15382485—
반응물2-(2-Chloro-6-nitrophenyl)ethoxycarbonyl chlorideHCID 19082692—
반응물N2 isopropanolHCID 86752769—
용매DichloromethaneHCID 6344—
생성물5'-O-(2-(2-chloro-6-nitrophenyl)ethoxycarbonyl)-N4-(2-(4-nitrophenyl)ethoxycarbonyl)-2'-deoxycytidineHCID 54456412680%

반응 조건

온도-60 °C

반응 단계

N4 -(2-(4-nitrophenyl)ethoxycarbonyl)-2'-deoxycytidine (5 g, 11.9 mmol) was co-evaporated with pyridine (2×60 ml, pro analysi quality, additionally dried over molecular sieve 4 Å), dissolved in pyridine (60 ml, see above) and cooled to -60° C. (i-PrOH/N2). A solution of 2-(2-chloro-6-nitrophenyl)ethoxycarbonyl chloride (4.7 g, 17.8 mmol) in CH2Cl2 (60 ml, dist. over CaH2) was added dropwise thereto for 75 min and was stirred for 1 h 45 min in conditions of i-PrOH/N2 cooling (-40° to -25° C.). The mixture was diluted with CH2Cl2 (150 ml) and washed with H2O (100 ml). The aqueous phases were post-extracted with CH2Cl2 (100 ml). Drying the organic phases over Na2SO4, filtering, evaporating the solvent under reduced pressure and co-evaporating with toluene (3×50 ml) yielded the crude product (9.8 g) which was purified by column chromatography (440 g SiO2, 32×5.9 cm, solvent: CH2Cl2 /MeOH 100:4). 5'-O-(2-(2-chloro-6-nitrophenyl)ethoxycarbonyl)-N4 -(2-(4-nitrophenyl)ethoxycarbonyl)-2'-deoxycytidine (5.247 g, 680%) was obtained as a colourless foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763599
출처 데이터셋uspto-grants-1998_06
ORD IDord-9615d9b765264c8cb6f5b0a1a99b2403
출처 메모uspto-grants-1998_06