Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Iodoisatin | HCID 88695 | — |
| Reactant | HCID 2743890 | HCID 2743890 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178517218 | HCID 178517218 | 79% |
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-[(2-chlorophenoxy)methyl]-1,3-thiazole-4-carbohydrazide. 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 47 mg of the title compound (79%) as a orange powder in 98.2% purity by HPLC (Rt: 5.07, 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-9435a03b265e4a47898f492a39714d05 |
|---|
| Source note | uspto-grants-2010_04 |
|---|