In the synthetic route, the nitro group at the 5-position provides a handle for subsequent reduction to an amino group, which is then functionalized to form the heterocyclic core of Tucatinib. The isatin scaffold contributes to the fused-ring system critical for HER2 receptor binding. Following these transformations, additional coupling reactions and functional group modifications are carried out to generate the final Active Pharmaceutical Ingredient. 5-Nitroisatin is a key intermediate employed to synthesize Tucatinib.
5-Nitroisatin
| API Name | Tucatinib |
|---|---|
| CAS No | 611-09-6 |
| Molecular Formula | C8H4N2O4 |
| Molecular Weight | 192.13 g/mol |
| Synonyms | 5-nitro-1H-indole-2,3-dione |
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Frequently Asked Questions
In the synthetic route, the nitro group at the 5-position provides a handle for subsequent reduction to an amino group, which is then functionalized to form the heterocyclic core of Tucatinib. The isatin scaffold contributes to the fused-ring system critical for HER2 receptor binding. Following these transformations, additional coupling reactions and functional group modifications are carried out to generate the final Active Pharmaceutical Ingredient. 5-Nitroisatin is a key intermediate employed to synthesize Tucatinib.
The CAS number of 5-Nitroisatin is 611-09-6.
The molecular formula of 5-Nitroisatin is C8H4N2O4.
The listed molecular weight of 5-Nitroisatin is 192.13 g/mol.
5-Nitroisatin is listed as being used in connection with the following API: Tucatinib.
The listed synonym or IUPAC name for 5-Nitroisatin is 5-nitro-1H-indole-2,3-dione.