Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Glycerol | HCID 753 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 4-Aminopyridine | HCID 1727 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Sodium 3-nitrobenzenesulfonate | HCID 31389 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1,6-Naphthyridine | HCID 67488 | — |
Reaktionsschritte
A sulfuric acid solution was prepared by adding H2SO4 (100 mL) to H2O (57 mL) cooled in an ice bath. To this solution was added glycerol (33 mL, 457 mmol), m-nitrobenzene sulfonic acid sodium salt (48 g, 212 mmol) and 4-amino-pyridine (10 g, 106 mmol). The reaction mixture was heated at 135° C. for 4 hours. The cooled reaction mixture was basicified with 2.5 N NaOH (500 mL) with cooling in an ice bath, and extracted into CH2Cl2 (3×200 mL). The organic fractions were combined, dried over Na2SO4 and concentrated. The resulting oil was purified by column chromatography (5% MeOH/CH2Cl2) affording 5.04 g (36%) as a dark orange oil. An analytical sample was prepared as the HCl salt from EtOAc yielding an orange low melting solid. MS EI m/z 130 M+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06465482B2 |
|---|
| Quelldatensatz | uspto-grants-2002_10 |
|---|
| ORD ID | ord-6e54163d303b4fd294b682c67d1ff5b0 |
|---|
| Quellennotiz | uspto-grants-2002_10 |
|---|