HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Piperidine → 2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 2-Oxoindoline-5-sulfonamide | HCID 10198232 | — |
| Edukt | 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde | HCID 22042092 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amide | HCID 69344083 | 80% |
Reaktionsbedingungen
| Temperatur | 90 °C |
|---|
Reaktionsschritte
A mixture of 2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide (28 mg, 0.13 mmol), 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde (34 mg, 0.13 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 90° C. for 2 hours. The reaction was cooled at 0° C. for overnight. The precipitate was collected by vacuum filtration, washed with cold ethanol and dried to give 47 mg (80%) of the title compound as an orange solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07071332B2 |
| Quelldatensatz | uspto-grants-2006_07 |
| ORD ID | ord-19e07496845b43c59dc41f9f66a4c6b4 |
| Quellennotiz | uspto-grants-2006_07 |