Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | 4-Iodobenzenecarbohydrazide | HCID 306104 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178517203 | HCID 178517203 | 83% |
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 4-iodobenzohydrazide. 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 430 mg of the title compound (83%) as a yellow solid in 98.7% purity by HPLC (Rt: 6.19, 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-dbbcaed8a50b4f8a9b7bb118e907f6ff |
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| Source note | uspto-grants-2010_04 |
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