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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056523Generated: October 26, 2026

Methyl iodide → 6-Iodo-1-(2-methoxyethyl)-2-(methylthio)pyrimidin-4(1H)-one

https://huagongshe.com/reaction/1056523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-iodo-1-(2-methoxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-oneHCID 86684687—
SolventAcetonitrileHCID 6342—
Product6-Iodo-1-(2-methoxyethyl)-2-(methylthio)pyrimidin-4(1H)-oneHCID 8668468643.1%

Reaction Steps

To a stirring solution of 6-iodo-1-(2-methoxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (9.00 g, 28.83 mmol) in MeCN (200 mL) was added diisopropylethylamine (5.0 mL, 28.83 mmol) and iodomethane (9.0 mL, 144.17 mmol). The reaction mixture was stirred at room temperature for 18 hours, and concentrated in vacuo. The residue was partitioned ortioned between CH2Cl2 (200 mL) and 1N aqueous HCl (100 mL). The layers were separated and the organic layer was washed with brine (100 mL), dried over MgSO4 and concentrated in vacuo. The resulting residue was purified by hot trituration with CH2Cl2/heptane to give the title compound (4.05 g, 43%) as a cream colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399626B2
Source datasetuspto-grants-2016_07
ORD IDord-348b65b96d28408c9206971450b1cd74
Source noteuspto-grants-2016_07