Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromoisatin | HCID 6889 | — |
| Reactant | HCID 178514418 | HCID 178514418 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178517025 | HCID 178517025 | 53% |
Reaction Steps
Following the general method as outlined in Example 1, into a suspension of 5-bromo-1H-indole-2,3dione in acetic acid was added 4-(1H-tetrazol-5-yl)benzohydrazide. 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 29 mg of the title compound (53%) as a orange Solid in 89.1% purity by HPLC (Rt: 3.29, gradient of 8 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-6538b5b5eb4f40a89512e592cbd12d68 |
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| Source note | uspto-grants-2010_04 |
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