HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535651Erstellt: 25. Oktober 2026
Lithium hydroxide, monohydrate → Lithium 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate
https://huagongshe.com/reaction/535651
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Edukt | Ethyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate | HCID 59636756 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Lithium 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate | HCID 66847495 | 99,3% |
Reaktionsschritte
Lithium hydroxide monohydrate (0.087 g, 2.08 mmol) was added to a solution of ethyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate (0.481 g, 1.04 mmol) in tetrahydrofuran (9 mL) and water (1 mL) and the reaction was heated at 100° C. for 35 min in a microwave oven. The solvents were evaporated and the material was dried in vacuum over P2O5 to give 0.454 g of the crude product. The crude material was used in the next step assuming quantitative yield without further purification. MS (ES+) m/z 434.2 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08859534B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-60b7f4463af14f0c8529a44db09bed08 |
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| Quellennotiz | uspto-grants-2014_10 |
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