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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164142Generated: October 27, 2026

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

https://huagongshe.com/reaction/1164142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
Reactant2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl-HCID 114682—
SolventEthanolHCID 702—
SolventDimethylacetamideHCID 31374—
ProductN4-butyloxycarbonyl-1-beta-D-arabinofuranosylcytosineHCID 1309027050%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367332
Source datasetuspto-grants-1983_01
ORD IDord-d7ea7f7b48384afca8aa126ee48a750b
Source noteuspto-grants-1983_01