HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl Beta-Carboline-3-Carboxylate → 3-(3-Cyclopropyl-1,2,4-oxadiazol-5-yl)-9H-beta-carboline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl Beta-Carboline-3-Carboxylate | HCID 105078 | — |
| Edukt | Cyclopropanecarboximidamide | HCID 431751 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-(3-Cyclopropyl-1,2,4-oxadiazol-5-yl)-9H-beta-carboline | HCID 18940725 | 52% |
Reaktionsschritte
To a solution of sodium ethoxide, prepared from sodium metal (0.6 g, 26 mmol) and anhydrous ethanol (50 mL), cyclopropylmethanimidamide (1.67 g, 16 mmol) and 9H-β-carboline-3-carboxylic acid ethyl ester (2.0 g, 8.0 mmol) were added. Toluene (50 mL) was added and the resulting mixture was heated to 120°-130° C. The ethanol and water formed during the reaction were removed by azeotropic distillation. The reaction was complete after 30 min. The solid was filtered from the reaction mixture, washed with water and dried. This afforded the title compound (1.15 g, 52%) as an yellow solid. M.p. 256°-257° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05834482 |
| Quelldatensatz | uspto-grants-1998_11 |
| ORD ID | ord-a5fa28fb02984bcaa1055039dc7cd15f |
| Quellennotiz | uspto-grants-1998_11 |