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HRID 1164142作成日:2026年10月27日

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

https://huagongshe.com/reaction/1164142

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Butyl chloroformateHCID 61140—
反応物2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl-HCID 114682—
溶媒EthanolHCID 702—
溶媒DimethylacetamideHCID 31374—
生成物N4-butyloxycarbonyl-1-beta-D-arabinofuranosylcytosineHCID 1309027050%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04367332
出典データセットuspto-grants-1983_01
ORD IDord-d7ea7f7b48384afca8aa126ee48a750b
出典メモuspto-grants-1983_01