HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407999Erstellt: 25. Oktober 2026
Potassium Carbonate → (S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/407999
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Methyl 3-fluoro-4-hydroxybenzoate | HCID 7019368 | — |
| Edukt | (R)-tert-butyl 4-(3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 86688072 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 86688102 | 83,3% |
Reaktionsschritte
(Step A: To a solution of (R)-tert-butyl 4-(3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (Preparation D; 2 g, 5.5 mmol) in DMF (20 mL) was added potassium carbonate (0.99 g, 7.2 mmol) and methyl 3-fluoro-4-hydroxybenzoate (1.1 g, 6.6 mmol) and the reaction was heated to 60° C. overnight. The reaction was diluted with water (100 mL) and extracted with EtOAc (100 mL). The organic layer was washed with 1 N NaOH (20 mL), and brine (20 mL), dried over MgSO4, filtered and concentrated under vacuum to give (S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (2 g, 83%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754226B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-665b604533a04a9f985e6a9fdb4eead0 |
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| Quellennotiz | uspto-grants-2014_06 |
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