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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749056Generated: November 3, 2026

Lithium iodide → (R)-4-(2-chloro-6-(iodomethyl)pyrimidin-4-yl)-3-methylmorpholine

https://huagongshe.com/reaction/1749056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
Reactant(R)-(2-chloro-6-(3-methylmorpholino)pyrimidin-4-yl)methyl methanesulfonateHCID 86651636—
Solvent1,4-DioxaneHCID 31275—
Product(R)-4-(2-chloro-6-(iodomethyl)pyrimidin-4-yl)-3-methylmorpholineHCID 7158455186%

Reaction Conditions

Temperature107 °C

Reaction Steps

(R)-(2-Chloro-6-(3-methylmorpholino)pyrimidin-4-yl)methyl methanesulfonate (80 g, 248.62 mmol) and lithium iodide (83 g, 621.54 mmol) were dissolved in dioxane (300 ml) and then heated at 107° C. for 1 hour. The reaction mixture was quenched with water (250 ml), extracted with EtOAc (3×250 ml), the organic layer was dried over MgSO4, filtered and evaporated. The residue was dissolved in DCM and Et2O was added, the mixture was passed through silica (4 inches) and eluted with Et2O. Fractions containing product were evaporated and the residue was then triturated with Et2O to give a solid which was collected by filtration and dried under vacuum to afford (R)-4-(2-chloro-6-(iodomethyl)pyrimidin-4-yl)-3-methylmorpholine (75 g, 86%); m/z: (ESI+) MH+, 354.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09155742B2
Source datasetuspto-grants-2015_10
ORD IDord-c64a96edcce044e4852003081999ef70
Source noteuspto-grants-2015_10