HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimide | HCID 68492812 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide | HCID 68488747 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745641B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-3a4194fa02704c5cae6b287a0ac883f5 |
| Source note | uspto-grants-2010_06 |