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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926133Generated: November 1, 2026

Methyl Methanesulfonate → 4,6-diiodo-N-methylpyrimidin-5-amine

https://huagongshe.com/reaction/1926133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl MethanesulfonateHCID 4156—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Diiodopyrimidin-5-amineHCID 11810154—
SolventTetrahydrofuranHCID 8028—
Product4,6-diiodo-N-methylpyrimidin-5-amineHCID 25186362—

Reaction Steps

To a solution of 4,6-diiodopyrimidin-5-amine (1.0 g) in tetrahydrofuran (10 mL) was added sodium hydride (60%, 138 mg) under ice-cooling. The mixture was stirred at room temperature for 30 min. To the reaction system was added dropwise a solution of methyl methanesulfonate (0.256 mL) in tetrahydrofuran (4.0 mL). The mixture was stirred at room temperature for 3 hrs and ethyl acetate was added. The mixture was washed with water and saturated brine and dried over magnesium sulfate. After concentration under reduced pressure, the residue was separated and purified by silica gel column chromatography (hexane:ethyl acetate=9:1→3:1) to give the title compound (600 mg) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-dacc69e5c2084dc7a9664fed5adcfcd7
Source noteuspto-grants-2012_05