HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11192Erstellt: 24. Oktober 2026
Hydrochloric Acid → Oleic acid-2-{[3-(4-amino-piperidin-1-yl)-propyl]-(2-oleoyloxy-ethyl)-amino}-ethyl ester
https://huagongshe.com/de/reaction/11192
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Edukt | Oleoyl chloride | HCID 5364783 | — |
| Edukt | 2-{[3-(4-Amino-piperidin-1-yl)-propyl]-(2-hydroxy-ethyl)-amino}-ethanol-hydrochloride | HCID 21967233 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Oleic acid-2-{[3-(4-amino-piperidin-1-yl)-propyl]-(2-oleoyloxy-ethyl)-amino}-ethyl ester | HCID 86590578 | — |
Reaktionsschritte
A suspension of 4.5 g (4 mmol) of the 2-{[3-(4-amino-piperidin-1-yl)-propyl]-(2-hydroxy-ethyl)-amino}-ethanol-hydrochloride described in example 10 in 100 ml dichloromethane is admixed with 3.5 g N-ethyl-diisopropylamine and 0.87 g (4 mmol) pyrocarbonic acid di-t-butyl ester, it is refluxed for 18 h, a solution of 2.4 g (8 mmol) oleoyl chloride in 40 ml dichloromethane is added dropwise, it is refluxed for 18 h, admixed with 15 ml etheric hydrogen chloride solution and stirred for 6 h at room temperature. It is concentrated by evaporation, adjusted to pH 9 with N sodium hydroxide solution, extracted with dichloromethane and methanol, dried and concentrated by evaporation. After chromatography on silica gel (eluting agent ethyl acetate/methanol 1:1) 1.1 g (36% of theory) of the title compound is isolated as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07097854B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-7afa7b65fe894f658bd2a222ed482b09 |
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| Quellennotiz | uspto-grants-2006_08 |
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