Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridiniumtribromideHCID 21124087—
Reactant7-nitro-1H-indole-2-carboxamideHCID 47319698—
SolventPyridineHCID 1049—
Product3-bromo-7-nitro-1H-indole-2-carboxamideHCID 6882515278.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566736B2
Source datasetuspto-grants-2009_07
ORD IDord-3027dac31ac64d04b08c638b60c63e7a
Source noteuspto-grants-2009_07