HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1501926Erstellt: 27. Oktober 2026
tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate
https://huagongshe.com/reaction/1501926
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 24820294 | — |
| Edukt | 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 59568715 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate | HCID 71271745 | — |
Reaktionsschritte
5-(Oxiran-2-yl)-2-benzofuran-1(3H)-one (1.5 g, 8.5 mmol) and commercially available (S)-4-N—BOC-2-hydroxymethyl piperazine (2.394 g, 11.07 mmol) were combined in ethanol (10 mL) in a microwave tube. The mixture was degassed then heated for 60 min at 150° C. LC-MS showed the product peak. The reaction was worked up by adding ethyl acetate and washing once with brine. The organic layer was separated, dried, and concentrated to dryness. The crude product was purified by MPLC using an 80 g Redi-sep column and eluted with 50%-100% EtOAc/hexane yielding the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09206199B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-46dab300aa3e4aba998386750e6c0722 |
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| Quellennotiz | uspto-grants-2015_12 |
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