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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053921Generated: October 30, 2026

Triethylamine → 6((2-Chloropyrimidin-4-yl)amino)hexahydrofuro[3,2-b]furan-3-ol

https://huagongshe.com/reaction/1053921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant6-Aminohexahydrofuro[3,2-b]furan-3-ol hydrochlorideHCID 118387959—
SolventEthanolHCID 702—
Product6((2-Chloropyrimidin-4-yl)amino)hexahydrofuro[3,2-b]furan-3-olHCID 11838796932%

Reaction Steps

To a suspension of 6-aminohexahydrofuro[3,2-b]furan-3-ol hydrochloride (363 mg, 2.0 mmol) in EtOH (10 mL) were added 2,4-dichloropyrimidine (298 mg, 2.0 mmol) and Et3N (1.01 g, 10.0 mmol) and the mixture was stirred at rt under nitrogen atmosphere overnight. The reaction mixture was filtered and washed with DCM (30 mL) and the filtrate was concentrated in vacuo. The residue was purified by silica gel chromatography (DCM/MeOH=30/1) to give the title compound as a white solid (165 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394281B2
Source datasetuspto-grants-2016_07
ORD IDord-43d7321e42e74c23bf96c9e329b700d1
Source noteuspto-grants-2016_07