Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | Acetic acid, (4-nitrophenoxy)-, hydrazide | HCID 156556 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178521414 | HCID 178521414 | 85% |
Reaction Steps
Following the general method as outlined in Example 1, into a suspension of 5-iodo-1H-indole-2,3-dione in acetic acid was added 2-(4-nitrophenoxy)acetohydrazide. 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 395 mg of the title compound (85%) as a yellow solid in 97.3% purity by HPLC (Rt: 5.76, gradient of 10 min, MaxPlot detection between 230 and 400 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696231B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6951eed442934de884b7b69f4a4ff9a0 |
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| Source note | uspto-grants-2010_04 |
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