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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888985Generated: October 29, 2026

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

https://huagongshe.com/reaction/888985

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 numberUS08252802B2
Source datasetuspto-grants-2012_08
ORD IDord-4c1d70b6fd8d49b0940f9e0135f4032a
Source noteuspto-grants-2012_08