HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20975Erstellt: 23. Oktober 2026
Acetic Acid → 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole
https://huagongshe.com/de/reaction/20975
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | Indole-5-carboxaldehyde | HCID 589040 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole | HCID 68489934 | 47% |
Reaktionsschritte
5-Formylindole (500 mg, 3.44 mmol) was dissolved in acetonitrile (10 mL), and the solution was added with 1-(tert-butoxycarbonyl)piperazine (961 mg, 5.16 mmol), acetic acid (3.90 mL, 68.1 mmol) and sodium triacetoxyborohydride (3.65 g, 17.2 mmol) little by little, followed by stirring at room temperature for 2 hours. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9, followed by extracting 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 flash column chromatography (hexane/ethyl acetate=19/1, 7/3, 1/1) to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole (505 mg, yield 47%).
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-40825bde11ad4d73a783930ebca6be83 |
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| Quellennotiz | uspto-grants-2010_06 |
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