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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749806Generated: November 2, 2026

Sodium Hydroxide → 6-Bromo-7-azaindole

https://huagongshe.com/reaction/1749806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzoyl-6-bromo-7-azaindoleHCID 15013893—
SolventMethanolHCID 887—
Product6-Bromo-7-azaindoleHCID 1115991595%

Reaction Steps

A solution of 1-benzoyl-6-bromo-1H-pyrrolo[2,3-b]pyridine (0.046 g, 0.15 mmol) in methanol (5.0 mL) was added with 5 N aqueous sodium hydroxide (1.0 mL), and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure, the residue was extracted with diethyl ether, and then the organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain 6-bromo-1H-pyrrolo[2,3-b]pyridine (0.028 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-fcaa67e39a4f4393b407b84726845077
Source noteuspto-grants-2015_10