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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21106Generated: October 26, 2026

Iodine → 3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide

https://huagongshe.com/reaction/21106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactant3-Amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimideHCID 68492812—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimideHCID 6848874782%

Reaction Steps

3-Amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phtalimide (300 mg, 0.795 mmol) was dissolved in ethanol (21 mL), and the solution was added with iodine (242 mg, 0.954 mmol) and silver sulfate (248 mg, 0.795 mmol), followed by stirring at room temperature for 1.3 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by slurry using chloroform to obtain 3-amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide (326 mg, yield 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-3a4194fa02704c5cae6b287a0ac883f5
Source noteuspto-grants-2010_06