Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77548Generated: October 26, 2026

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

https://huagongshe.com/reaction/77548

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 numberUS08841314B2
Source datasetuspto-grants-2014_09
ORD IDord-2ea1b69b5b644f17b66a4f77d405a6f5
Source noteuspto-grants-2014_09