Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | HCID 9813598 | HCID 9813598 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178517208 | HCID 178517208 | 81% |
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 N-[4-(hydrazinocarbonyl)phenyl]-2-furamide. 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 81 mg of the title compound (81%) as a yellow powder in 96.7% purity by HPLC (Rt: 4.05, gradient of 8 min, MaxPlot detection between 230 and 400 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07696231B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-252799c2960545b885e2f249456053e1 |
|---|
| Source note | uspto-grants-2010_04 |
|---|