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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842543Generated: October 31, 2026

Methyl iodide → 3-(4-Chloro-indazol-1-yl)-1-methyl-6-trifluoromethylpyrimidine-2,4-dione

https://huagongshe.com/reaction/842543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-chloro-indazol-1-yl)-6-trifluoromethyl-1H-pyrimidine-2,4-dioneHCID 22614262—
SolventAcetonitrileHCID 6342—
Product3-(4-Chloro-indazol-1-yl)-1-methyl-6-trifluoromethylpyrimidine-2,4-dioneHCID 1145079339.7%

Reaction Steps

A mixture of 168B (100 mg, 0.3 mmol), dry acetonitril (3 mL), potassium carbonate (0.05 g, 0.33 mmol) and methyl iodide (0.1 g, 0.7 mmol) is stirred overnight at room temperature. The solids are removed by filtration. The motherliquor is concentrated under reduced pressure. The residue obtained is purified by flash chromatography (ethyl acetate/petrol ether 3/7) which yields the product as an orange semi-solid (41 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376426B1
Source datasetuspto-grants-2002_04
ORD IDord-9c1a77e972fb40a085e49424b87461d6
Source noteuspto-grants-2002_04