Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946379Generated: November 2, 2026

Methyl iodide → HCID 59547867, compound

https://huagongshe.com/reaction/1946379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 59547990HCID 59547990—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 59547867HCID 59547867—

Reaction Steps

To a solution of 2,6-difluoro-N-(1-{[4-hydroxy-2-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide (for a preparation see Example 36)(72 mg, 0.181 mmol) in DMSO (0.5 ml) was added potassium t-butoxide (20 mg, 0.178 mmol). The reaction mixture was stirred for 5 min before adding methyl iodide (0.011 ml, 0.181 mmol, Aldrich). The reaction was stirred at ambient temperature, overnight and under nitrogen. The reaction mixture was filtered through a hydrophobic frit and the filtrate diluted with methanol (0.5 ml) and the sample purified by MDAP on Sunfire C18 column using Acetonitrile-Water with a Formic acid modifier (Method B). The solvent was evaporated in vacuo to give the title compound as a white solid (20.3 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-0f05e9a9687442e5af18d696e774b107
Source noteuspto-grants-2013_03