Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | HCID 178523802 | HCID 178523802 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Katalysator | Ferrate(4-), hexakis(cyano-C)-, tetrapotassium, (OC-6-11)- | HCID 11963580 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Sodium Chloride | HCID 5234 | — |
| Produkt | HCID 178509617 | HCID 178509617 | 43% |
Reaktionsschritte
N-{trans-4-[(8-Bromoquinolin-4-yl)oxy]cyclohexyl}-3-fluorobenzamide (500 mg, 1.13 mmol) (see example 12), sodium carbonate (120 mg, 1.13 mmol) and palladium(II) acetate (13 mg, 0.06 mmol) were dissolved in N,N-dimethylacetamide (23 mL) and finely triturated potassium hexacyanoferrate (105 mg, 2.5 mmol) was added. The reaction mixture was stirred under a nitrogen atmosphere for 3 hours at 120° C. After cooling to room temperature, the reaction mixture was diluted with water and saturated sodium chloride solution and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate, then the sodium sulphate and solvent residues were removed. After chromatography of the residue, the desired product was obtained at 43% yield (190 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09428460B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
|---|
| ORD ID | ord-cd7c415faf06465e9aaab6efe123a5b2 |
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| Quellennotiz | uspto-grants-2016_08 |
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