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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893891Generated: 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/1893891

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 numberUS08513266B2
Source datasetuspto-grants-2013_08
ORD IDord-9a7fd0f1803547b58b5240f6a42e52f1
Source noteuspto-grants-2013_08