HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370061Erstellt: 25. Oktober 2026
Melatonin → N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide
https://huagongshe.com/reaction/370061
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Melatonin | HCID 896 | — |
| Edukt | Borane | HCID 6331 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Trifluoroacetic acid | HCID 6422 | — |
| Produkt | N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide | HCID 23283701 | — |
Reaktionsschritte
To a solution, cooled to 0° C., of melatonin (1 mmol) in trifluoroacetic acid (2 ml) is added dropwise borane (2 eq, 1M solution in THF). The mixture is stirred for 30 min at 0° C. followed by dropwise addition of water (1.5 ml), and the medium is left stirring for 1 h at room temperature. The mixture is then brought to pH=10 using 2N potassium hydroxide solution and is then extracted with dichloromethane. The crude product is separated on a column of flash silica (25/75/5 acetone/dichloromethane/methanol) and 110 mg of N-[2-(5-methoxyindolin-3-yl)ethyl]acetamide are obtained, which product is then acetylated with acetic anhydride in pyridine to give N-[2-(1-acetyl-5-methoxyindolin-3-yl)ethyl]acetamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06140372 |
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| Quelldatensatz | uspto-grants-2000_10 |
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| ORD ID | ord-b487646d24224174922936a970b2bb5f |
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| Quellennotiz | uspto-grants-2000_10 |
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