HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethoxyacetyl chloride → 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethoxyacetyl chloride | HCID 84189 | — |
| Edukt | 7-bromo-N4-isobutylquinoline-3,4-diamine | HCID 68818159 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline | HCID 21984386 | 41,1% |
Reaktionsschritte
A solution of 7-bromo—N4-isobutylquinoline-3,4-diamine (85 g, prepared according to Part F of Example 1) in anhydrous pyridine (413 mL) was immersed in an ice bath, and ethoxyacetyl chloride (36.9 g, 300 mmol) was added. The reaction was allowed to warm to room temperature and was then heated in an oil bath held at 85° C. for 3.5 h. The reaction mixture was concentrated under vacuum, and the residue was taken up in diethyl ether and washed with 2M Na2CO3 (2×) followed by H2O (1×). The organic layer was dried (MgSO4), filtered, and concentrated. Recrystallization of the resulting solid from boiling 15% ethyl acetate in hexanes afforded 43.0 g of 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline as brown crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091214B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-dbeb3e2c5d2e43e88e3b4fdfc8b56049 |
| Quellennotiz | uspto-grants-2006_08 |