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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511836Generated: November 1, 2026

Methyl iodide → methyl 1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/511836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 6-(trifluoromethyl)-1H-indazole-3-carboxylateHCID 53408454—
SolventAcetonitrileHCID 6342—
Productmethyl 1-methyl-6-(trifluoromethyl)-1H-indazole-3-carboxylateHCID 6729140375%

Reaction Steps

To an acetonitrile (5 ml) solution of methyl 6-(trifluoromethyl)-1H-indazole-3-carboxylate (300 mg, 1.2 mmol) were added potassium carbonate (1.0 g, 7.4 mmol) and iodomethane (350 mg, 2.5 mmol) at room temperature respectively. The mixture was stirred at room temperature for 4 hours. The solid was removed by filtration and washed with acetonitrile. The filtrate was concentrated in vacuo. After being filtered off, the filtrate was concentrated under reduced pressure, the residue was applied to a silica gel chromatography column and eluted with a hexane/ethyl acetate=4/1 to furnish 239 mg (75% yield, major product) of the title as a white solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101616B2
Source datasetuspto-grants-2015_08
ORD IDord-36f0a09e9c9e4e4ebee205de62538e82
Source noteuspto-grants-2015_08