Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Bromoisatin | HCID 6889 | — |
| Edukt | 4-Methoxybenzohydrazide | HCID 76792 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | HCID 178491622 | HCID 178491622 | 57% |
Reaktionsschritte
Following the general method as outlined in Example 1, into a suspension of 5-bromo-1H-indole-2,3-dione in acetic acid was added 4-methoxybenzohydrazide. After stirring at 100° C., the reaction mixture was cooled to rt and a yellow solid precipitated out. Filtration on a fritté, washing with AcOH, water and drying under vacuo at 60° C. overnight gave 53 mg of the title compound (57%) as a orange powder in 93% purity by HPLC (Rt: 4.11, gradient of 8 min, MaxPlot detection between 230 and 400 nm).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07696231B2 |
|---|
| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-9d26efb736ee445988ba61e863dcb111 |
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| Quellennotiz | uspto-grants-2010_04 |
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