HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 2-Chloro-6-methoxyquinoline | HCID 83647 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 1-Benzyl-2-piperidone | HCID 5170076 | — |
| Produkt | 1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-ol | HCID 58181126 | — |
Reaktionsbedingungen
| Temperatur | -78 °C |
|---|
Reaktionsschritte
Under an argon atmosphere 14.0 mL (28.0 mmol) of a 2 M lithium diisopropylamide solution in 50 mL THF were cooled to −78° C. and combined with stirring with a solution of 5.00 g (25.1 mmol) of 2-chloro-6-methoxy-quinoline in THF. After 1 h stirring at −78° C., 4.5 mL (25.2 mmol) N-benzylpiperidone were added dropwise. After 1 h stirring at −78° C. the mixture was allowed to come up to RT and stirred overnight. The mixture was evaporated down i. vac. and purified by flash chromatography through Alox. The fractions containing the product were combined and evaporated down.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08629137B2 |
| Quelldatensatz | uspto-grants-2014_01 |
| ORD ID | ord-86951bac4dce423987c5afaee4886243 |
| Quellennotiz | uspto-grants-2014_01 |