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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267346Generated: October 30, 2026

Morpholine → 4-(5-(4-Fluorobenzyl)-4-(2-morpholinoethyl)thiophen-2-yl)-5-chloro-2-(methylthio)pyrimidine

https://huagongshe.com/reaction/2267346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-(4-Fluoro-benzyl)-5-(5-chloro-2-(methylthio)pyrimidin-4-yl)thiophen-3-yl)ethanolHCID 60204463—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product4-(5-(4-Fluorobenzyl)-4-(2-morpholinoethyl)thiophen-2-yl)-5-chloro-2-(methylthio)pyrimidineHCID 6020446474.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methanesulfonyl chloride (59 mg, 0.52 mmol) was added to a mixture of 2-(2-(4-fluoro-benzyl)-5-(5-chloro-2-(methylthio)pyrimidin-4-yl)thiophen-3-yl)ethanol (170 mg, 0.43 mmol) and diisopropylethylamine (72 mg, 0.55 mmol) in dichloromethane (8 mL) at 0° C. After stirring at 0° C. for 1 h, the solvent was removed in vacuo. Acetonitrile (5 mL) and morpholine (112 mg, 1.29 mmol) were added to the residue and the mixture was heated to 70° C. overnight. After cooling to rt solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with methanol (1 M ammonia)/dichloromethane (1:20) to afford the title compound (148 mg, 74%). MS (M+H)+ 464/466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-ccab02cf9a8f441e9a4b41250539062e
Source noteuspto-grants-2010_12