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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243242Generated: November 2, 2026

3-(1,1-Dimethyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-1-one → N1-[4-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-methylphenyl]-N2-(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamide

https://huagongshe.com/reaction/2243242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1,1-Dimethyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-1-oneHCID 59030676—
Reactant1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazoleHCID 59210395—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventAcetonitrileHCID 6342—
ProductN1-[4-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-methylphenyl]-N2-(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamideHCID 5921039193.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-(1,1-Dimethyl-2-methylsulfanyl-ethylimino)-4-iodo-3H-isobenzofuran-1-one (0.53 g) and 1-(3-methyl-4-aminobenzyl)-3,5-bis(trifluoromethyl)-1H-pyrazole (0.45 g) were dissolved in acetonitrile (15 ml), to which p-toluenesulfonic acid monohydrate (0.01 g) was added and the mixture was stirred at 60° C. for 3 hours. After finishing the reaction, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography to obtain N1-[4-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-methylphenyl]-N2-(1,1-dimethyl-2-methylsulfanylethyl)-3-iodophthalamide (0.91 g). mp. 83-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674807B2
Source datasetuspto-grants-2010_03
ORD IDord-bb6e2c81ffef4710ba047869401035b7
Source noteuspto-grants-2010_03