Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357024Generated: October 30, 2026

Chloroacetaldehyde → 5-(4-Hydroxybutylthio)imidazo[1,2-c]pyrimidine

https://huagongshe.com/reaction/357024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant4-Amino-2-(4-hydroxybutylthio)pyrimidineHCID 18936811—
SolventEthanolHCID 702—
Product5-(4-Hydroxybutylthio)imidazo[1,2-c]pyrimidineHCID 18936882—

Reaction Steps

To a solution of 4.98 g (25 mmol) of 4-amino-2-(4-hydroxybutylthio)pyrimidine in 70 ml of ethanol, 30 ml of a 40% chloroacetaldehyde solution was added, followed by refluxing for 4 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in chloroform, washed with saturated aqueous sodium hydrogen carbonate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, n-hexane/ethyl acetate=1/1→1/4→ethyl acetate) to yield 3.15 g (56.4%, white crystal) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-b32d3089c842437fb6246ce71bf7e620
Source noteuspto-grants-1998_11