HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → N-[3-(5-isopropyl-4-methoxy-2-methylbenzylidene)-2-oxo-2,3-dihydro-1H-indol-6-yl]-acetamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Pyrrolidine | HCID 31268 | — |
| Edukt | N-(2-Oxoindolin-6-yl)acetamide | HCID 2749839 | — |
| Edukt | 5-Isopropyl-4-methoxy-2-methylbenzaldehyde | HCID 3276129 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-[3-(5-isopropyl-4-methoxy-2-methylbenzylidene)-2-oxo-2,3-dihydro-1H-indol-6-yl]-acetamide | HCID 57270199 | 70% |
Reaktionsschritte
A mixture of 5-isopropyl-4-methoxy-2-methylbenzaldehyde (0.25 g, 1.3 mmol), 6-acetamido-2-oxindole (0.25 g, 1.3 mmol) and pyrrolidine (0.54 ml, 6.5 mmol) in ethanol (4 ml) was held in a sealed tube at 100° C. for 12 hours. The reaction was cooled and then poured into water (100 ml). The solid which formed was removed by filtration, washed with water and then dissolved in ethyl acetate (200 ml). The ethyl acetate solution was dried over magnesium sulfate and concentrated. The resulting solid was triturated with dichloromethane/hexanes to afford 0.33 g (70%) of N-[3-(5-isopropyl-4-methoxy-2-methylbenzylidene)-2-oxo-2,3-dihydro-1H-indol-6-yl]-acetamide as a brownish yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06855730B2 |
| Quelldatensatz | uspto-grants-2005_02 |
| ORD ID | ord-e98db52dd1d24397b55062fec6a0fdab |
| Quellennotiz | uspto-grants-2005_02 |