HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106932Erstellt: 24. Oktober 2026
Tryptamine → (R/S)-1-(1-adamantyl)methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole
https://huagongshe.com/de/reaction/1106932
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tryptamine | HCID 1150 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 2-(Adamantan-1-yl)acetaldehyde | HCID 5086084 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R/S)-1-(1-adamantyl)methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole | HCID 53933490 | — |
Reaktionsschritte
Trifluoroacetic acid (443 μl, 5.8 mmol) was added to a solution of tryptamine (5.76 g, 36 mmol) and 1-adamantylacetaldehyde (6.52 g, 36.6 mmol) in dry DCM (450 ml) wth 3A molecular sieves (46.5 g) at 0° C. The reaction mixture was stirred at 0° C. for 2 hours, followed by the addition of trifluoroacetic acid (5.76 ml, 74.8 mmol) then allowed to warm to room temperature and stirring continued for a further 16 hours. The resultant suspension was concentrated in vacuo, taken up in ethyl acetate (200 ml), filtered, washed successively with saturated NaHCO3 solution (200 ml), brine (2×200 ml) and dried (MgSO4). Filtration and evaporation of the solvent gave the crude product as an orange foam which was used without further purification. (10.95 g, 95%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06057311 |
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| Quelldatensatz | uspto-grants-2000_05 |
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| ORD ID | ord-52e02d18810840879caff7db30fc6329 |
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| Quellennotiz | uspto-grants-2000_05 |
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