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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79016Generated: November 3, 2026

Iodine chloride → 4-(2-Fluoro-4-iodophenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/79016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
Reactant4-(2-Fluoro-4-trimethylsilanylphenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl esterHCID 67083987—
SolventDichloromethaneHCID 6344—
Product4-(2-Fluoro-4-iodophenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl esterHCID 6708409083%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(2-fluoro-4-trimethylsilanylphenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl ester (0.56 g, 1.1 mmol) in DCM (3 mL) at 0° C. was added a solution of iodine monochloride in DCM (2.2 mL, 1M, 2.2 mmol). The reaction mixture was stirred at 0° C. for 30 minutes. The reaction was quenched by the addition of water (10 mL) then diluted with saturated aqueous sodium thiosulfate solution (10 mL). The resultant mixture was extracted with ethyl acetate (3×20 mL) and the combined organic fractions washed with brine (20 mL), dried (MgSO4) then concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 0-100% DCM in cyclohexane) to yield the title compound as a light brown solid (0.51 g, 83%). LCMS (Method B): RT=4.87 min, [M+H]+=566.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-4246e28526fd4a2daa3987a8eb8ce992
Source noteuspto-grants-2014_09