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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21108Generated: October 25, 2026

Iodine → 4-Chloro-7-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]isoindolinone

https://huagongshe.com/reaction/21108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Chloro-7-(1-(tert-butoxycarbonyl)indol-2-yl)isoindolinoneHCID 68487594—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product4-Chloro-7-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]isoindolinoneHCID 6849220436%

Reaction Steps

In a similar manner to Step 1 of Example 161, 4-chloro-7-(1-(tert-butoxycarbonyl)-indol-2-yl)isoindolinone (374 mg, 0.980 mmol) was dissolved in ethanol (26 mL), and the solution was treated with iodine (299 mg, 1.18 mmol) and silver sulfate (306 mg, 0.980 mmol), followed by purification by slurry using hexane and diisopropylether to obtain 4-chloro-7-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]isoindolinone (179 mg, yield 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-e091ca1a6fd64562984b79a3781fd88c
Source noteuspto-grants-2010_06