Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | HCID 2730031 | HCID 2730031 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178521268 | HCID 178521268 | 76% |
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-[5-(4-morpholinyl)-2H-tetrazol-2-yl]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 73 mg of the title compound (76%) as a yellow powder in 86.7% purity by HPLC (Rt: 3.84, 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-e388bd820ce343309e68202954597807 |
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| Source note | uspto-grants-2010_04 |
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