Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 3-Methylfuran | HCID 13587 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | Oxindole | HCID 321710 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 66772244 | HCID 66772244 | 25,3% |
Reaktionsschritte
A solution of POCl3 (0.60 mL, 7.08 mmol) in DMF (0.65 mL, 8.431 mmol) was stirred at rt for 1 h. The reaction was cooled to 0° C. and added 3-methylfuran (490 mg, 5.97 mmol) dropwise. The mixture was stirred at 0 C for 1 h and at 40 C for additional 40 min. The reaction mixture was poured into H2O (25 mL), neutralized (Na2CO3), and extracted with EtOAc (25 mL×5). The organic layer was washed with brine, dried over Na2SO4 and concentrated. The crude material was heated at reflux with oxindole (800 mg, 6.02 mmol) and piperidine (0.60 mL, 8.08 mmol) in EtOH (5 mL) for 3 h. The resulting precipitate was collected by filtration to yield the desired 3-((3-methylfuran-2-yl)methylene)indolin-2-one (340 mg). LCMS (ES): m/z 226 [M+1]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08124649B2 |
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| Quelldatensatz | uspto-grants-2012_02 |
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| ORD ID | ord-dfff84b0d0214ac1b9cce94e054bf1f8 |
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| Quellennotiz | uspto-grants-2012_02 |
|---|