HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2233368Erstellt: 24. Oktober 2026
2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione → 2-{4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-3-hydroxybutyl}-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/de/reaction/2233368
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione | HCID 339433 | — |
| Edukt | 4-(3,4-Dichlorophenoxy)piperidine | HCID 3732042 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-{4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-3-hydroxybutyl}-1H-isoindole-1,3(2H)-dione | HCID 59296049 | 36,2% |
Reaktionsschritte
A mixture of 4-(3,4-dichlorophenoxy)piperidine (WO 0058305, WO 0177101) (4.40 g) and 2-(2-oxiran-2-ylethyl)-1H-isoindole-1,3(2H)-dione (J. Med. Chem. 1979, 22(6), 631-9. 5.00 g) in ethanol (50 ml) was stirred at 60° C. for 12 h. The mixture was cooled down and left overnight. The formed crystals were collected by filtration, washed with cold ethanol and dried under vacuum to afford the sub-title compound as a white solid (3.0 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07709500B2 |
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| Quelldatensatz | uspto-grants-2010_05 |
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| ORD ID | ord-7b0a51debb4a4553a01f0c4cebb620a5 |
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| Quellennotiz | uspto-grants-2010_05 |
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