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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053927Generated: November 1, 2026

Triethylamine → 2-((6-((2,5-Dichloropyrimidin-4-yl)amino)hexahydrofuro[3,2-b]furan-3-yl)oxy)ethanol

https://huagongshe.com/reaction/1053927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4,5-TrichloropyrimidineHCID 237259—
Reactant2-((6-Aminohexahydrofuro[3,2-b]furan-3-yl)oxy)ethanolHCID 118387954—
SolventEthanolHCID 702—
Product2-((6-((2,5-Dichloropyrimidin-4-yl)amino)hexahydrofuro[3,2-b]furan-3-yl)oxy)ethanolHCID 11838799316%

Reaction Steps

To a suspension of 2,4,5-trichloropyrimidine (0.71 g, 3.88 mmol) in EtOH (20 mL) were added 2-((6-aminohexahydrofuro[3,2-b]furan-3-yl)oxy)ethanol (crude product) and N,N-diethylethanamine (1.10 mL, 7.89 mmol). The mixture was stirred at room temperature overnight and concentrated in vacuo. The residue was purified by silica chromatography (DCM/MeOH (v/v)=50/1) to give the title compound as brown liquid (0.21 g, 16%, for three steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394281B2
Source datasetuspto-grants-2016_07
ORD IDord-0267adca91bf4b0387b1fb03ac2f1c0c
Source noteuspto-grants-2016_07