Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | HCID 2801744 | HCID 2801744 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178497995 | HCID 178497995 | 73% |
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 methyl 6-(hydrazinocarbonyl)nicotinate. 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 33 mg of the title compound (73%) as a yellow solid in 89.7% purity by HPLC (Rt: 4.44, 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-4ca403c539ae4d52b490b2e60b1e0db6 |
|---|
| Source note | uspto-grants-2010_04 |
|---|