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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271220Generated: November 3, 2026

Acetaldehyde → HCID 18452869, compound

https://huagongshe.com/reaction/1271220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPyrimidin-5-amineHCID 344373—
Reactant1368022-07-4HCID 69472207—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 18452869HCID 18452869—

Reaction Steps

A suspension of the 5-aminopyrimidine, and one twenty-fifth an equal mass of PtO2, and 5 equivalents equivalents of aqueous acetaldehyde, in ethanol solvent, was shaken under 60 psi hydrogen gas for 24 h. At this time, TLC of an evaporated aliquot of the reaction mixture indicated complete conversion of the 5-(N-ethyl)aminopyrimidine. The Pt catalyst was removed by filtering the reaction mixture through Celite, and the 5-(N,N-diethyl)aminopyrimidine was isolated by evaporation of the ethanol solvent. The crude product was purified by flash chromatography on silica using EtOAc/hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205310B2
Source datasetuspto-grants-2007_04
ORD IDord-d24865bc7b22419b8a1bf849372426e2
Source noteuspto-grants-2007_04