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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666253Generated: October 31, 2026

[4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidin-5-yl]methanol → 4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1666253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidin-5-yl]methanolHCID 57606985—
CatalystManganese oxideHCID 160959—
SolventChloroformHCID 6212—
Product4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehydeHCID 5760695393.6%

Reaction Steps

To a solution of [4-(ethylamino)-6-methyl-2-(methylthio)pyrimidin-5-yl]methanol (41.0 g) in chloroform (4000 mL) was added manganese oxide (125 g, 1.4 mole) and stirred for 4 h at room temperature. More manganese oxide was added until the disappearance of alcohol compound was observed. The reaction mixture was filtered through Celite and washed with some chloroform and evaporated all organic solvents to give 38 g (92% yield) of 4-(ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehyde as a colorless solid, which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044062B2
Source datasetuspto-grants-2011_10
ORD IDord-4f934987f5124f18b77249a762386bb5
Source noteuspto-grants-2011_10