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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164142생성일: 2026년 10월 26일

Triethylamine → N4-butyloxycarbonyl-1-beta-D-arabinofuranosylcytosine

https://huagongshe.com/reaction/1164142

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butyl chloroformateHCID 61140—
반응물2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl-HCID 114682—
용매EthanolHCID 702—
용매DimethylacetamideHCID 31374—
생성물N4-butyloxycarbonyl-1-beta-D-arabinofuranosylcytosineHCID 1309027050%

반응 단계

To a solution of 4.0 g of arabinofuranosylcytosine dissolved in 50 ml of dimethylacetamide, there are added 5.0 g of triethylamine and 3.37 g of butyloxycarbonyl chloride. The reaction is carried out by stirring the mixture at room temperature for 3 hours. After completion of the reaction, the solvent is evaoprated under reduced pressure. The residue is diluted with 20 ml of ethanol, followed by addition of 150 ml of petroleum ether. After the mixture is stirred at 0° to 5° C. for one hour, the resultant precipitates are collected by filtration. The precipitates are dissolved in 15 ml of methanol and then 100 ml of water is added to the resultant solution. The mixture is left to stand in a refrigerator and the precipitated crystals are filtered to give 2.8 g of N4 -butyloxycarbonyl-1-β-D-arabinofuranosylcytosine (Yield:50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04367332
출처 데이터셋uspto-grants-1983_01
ORD IDord-d7ea7f7b48384afca8aa126ee48a750b
출처 메모uspto-grants-1983_01