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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886787Generated: November 1, 2026

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

https://huagongshe.com/reaction/886787

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 numberUS08247408B2
Source datasetuspto-grants-2012_08
ORD IDord-be2788b1b3cd44279d34e48ce3ada367
Source noteuspto-grants-2012_08