Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Morpholine-4-carboximidamide Hydrobromide | HCID 2806564 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate | HCID 53395404 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 46253561 | HCID 46253561 | — |
Reaktionsschritte
To a 500 ml round bottom flask charged with anhydrous EtOH (150 ml) under nitrogen at 0° C. are added morpholine-4-carboxamidine hydrobromide (10.50 g, 50 mmol), tert-butyl-3-[(dimethylamino)methylene]-4-oxo-1-piperidinecarboxylate (12.7 g, 50 mmol, 1.0 eq.), and potassium t-butoxide in t-butanol (11.0M, 100 ml, 100 mmol, 2.0 eq.). The resulting mixture is stirred at 75° C. for 16 hr. The solvent is evaporated under reduced pressure, and the residue is taken up in DCM (300 ml), washed with water and brine, dried (Na2SO4) and concentrated. The residue is purified by silica gel chromatography (Hexane/EtOAc 1:1) to give the title compound. MS (+VE) m/z 321.1 (M++1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07795262B2 |
|---|
| Quelldatensatz | uspto-grants-2010_09 |
|---|
| ORD ID | ord-7a1b2c88050e4b0d8a190e35d0435036 |
|---|
| Quellennotiz | uspto-grants-2010_09 |
|---|