HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21107Erstellt: 24. Oktober 2026
Water → 3-Amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide
https://huagongshe.com/de/reaction/21107
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 3-Butyn-1-OL | HCID 13566 | — |
| Edukt | 3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide | HCID 68488747 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Diethylamine | HCID 8021 | — |
| Produkt | 3-Amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide | HCID 68492778 | 87% |
Reaktionsschritte
3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide (150 mg, 0.298 mmol) was dissolved in diethylamine (7.5 mL), and the solution was added with bis(triphenylphosphine)dichloropalladium (16.7 mg, 0.0234 mmol), copper iodide (11.4 mg, 0.0596 mmol) and 3-butyn-1-ol (0.226 mL, 2.98 mmol), followed by stirring at 50° C. for 3.7 hours under argon atmosphere. 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 preparative thin-layer chromatography (chloroform/methanol=10/1) to obtain 3-amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide (115 mg, yield 87%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745641B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-5cb5ea9590ec49be94d9bad2c5ae3039 |
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| Quellennotiz | uspto-grants-2010_06 |
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