HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium hydride → 3-amino-1-(2-methoxyethyl)-3,4-dihydroquinolin-2(1H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Edukt | 3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1) | HCID 13499428 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-amino-1-(2-methoxyethyl)-3,4-dihydroquinolin-2(1H)-one | HCID 21906837 | 78% |
Reaktionsschritte
Sodium hydride (60% in oil, 321 mg, 8.03 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (J. Med. Chem., 28, 1985; 1511–16; 759 mg, 3.82 mmol) in anhydrous DMF (10 mL) at 0° C. over a period of 5 min. After 1 hour 2-bromoethyl methyl ether (0.40 mL, 4.20 mmol) was added and stirring maintained for 18 hours. The reaction was diluted with EtOAc (100 mL) and washed with sat. aqueous K2CO3 (20 mL). The aqueous was extracted with DCM (3×50 mL) and the combined organics dried (Na2SO4), filtered and evaporated. The residue was purified by column chromatography (DCM to DCM:MeOH (4:1)) to afford the title compound (654 mg, 78%) as a brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07129249B2 |
| Quelldatensatz | uspto-grants-2006_10 |
| ORD ID | ord-8cdf941be0934c8e8835f9631b9965f6 |
| Quellennotiz | uspto-grants-2006_10 |