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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706043Generated: November 1, 2026

Methyl iodide → 2-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}-5-{[(5-ethyl-1-methyl-4-oxo-1,4-dihydro-2-pyrimidinyl)thio]methyl}benzonitrile

https://huagongshe.com/reaction/706043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178437208HCID 178437208—
SolventDichloromethaneHCID 6344—
Product2-{[4-Chloro-3-(trifluoromethyl)phenyl]oxy}-5-{[(5-ethyl-1-methyl-4-oxo-1,4-dihydro-2-pyrimidinyl)thio]methyl}benzonitrileHCID 6777566532.4%

Reaction Steps

To a suspension of 2-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}-5-{[(5-ethyl-4-oxo-1,4-dihydro-2-pyrimidinyl)thio]methyl}benzonitrile (120 mg, 0.258 mmol) and DIPEA (0.090 ml, 0.515 mmol) in DCM (2 mL) was added MeI (0.02416 ml, 0.386 mmol). The mixture was stirred at room temperature for 2 h. The reaction was then quenched with water, extracted with EA. The combined organic layers were dried with Na2SO4, filtered, concentrated and purified via reverse phase flash chromatography to afford the title compound (40 mg, 32.4% yield). LCMS: rt=3.44 min, [M+H+]=480

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-35de367426304a7daa54133320beff1b
Source noteuspto-grants-2015_11