Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromoisatin | HCID 6889 | — |
| Reactant | HCID 9964555 | HCID 9964555 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178497968 | HCID 178497968 | 34% |
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 methyl 3-(2-hydrazino-2-oxoethoxy)benzoate. 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 39 mg of the title compound (34%) as a orange powder in 97.5% purity by HPLC (Rt: 4.26, 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-58459bf350814ba98b57402df91b050f |
|---|
| Source note | uspto-grants-2010_04 |
|---|