HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230566Generated: November 1, 2026
Pyridiniumtribromide → 3-bromo-7-nitro-1H-indole-2-carboxamide
https://huagongshe.com/reaction/230566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | 7-nitro-1H-indole-2-carboxamide | HCID 47319698 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-bromo-7-nitro-1H-indole-2-carboxamide | HCID 68825152 | 78.9% |
Reaction Steps
A suspension of 2.57 g (12.53 mmol) of 7-nitro-1H-indole-2-carboxamide in 35 ml of pyridine is cooled to 0° C. in a water/ice bath. A solution of 4.01 g (12.53 mmol) of pyridinium tribromide in 20 ml of pyridine is then added at 0° C. dropwise, and the reaction is then stirred at 0° C. for 30 minutes and at ambient temperature for 16 h. 70 ml of ice-cold water are then added to the reaction medium. The latter is then stirred at ambient temperature for 15 minutes and is then filtered over sintered glass, to give 2.81 g of 3-bromo-7-nitro-1H-indole-2-carboxamide in the form of a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566736B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-3027dac31ac64d04b08c638b60c63e7a |
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| Source note | uspto-grants-2009_07 |
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