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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901408Generated: October 30, 2026

Benzoyl chloride → (5-bromo-1H-pyrrolo[2,3-b]pyridine-3-yl)-phenyl-methanone

https://huagongshe.com/reaction/901408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDichloromethaneHCID 6344—
Product(5-bromo-1H-pyrrolo[2,3-b]pyridine-3-yl)-phenyl-methanoneHCID 1130105940%

Reaction Steps

To a suspension of AlCl3 (338 mg, 2.54 mmol) in dichloromethane (10 mL) was added 5-bromo-1H-pyrrolo[2,3-b]pyridine (100 mg, 0.507 mmol). After stirring for 45 min, benzoyl chloride (0.3 mL, 2.54 mmol) was added and the reaction mixture was stirred for 3 h, before quenching with MeOH at 0° C. The mixture was concentrated in vacuum, the pH was changed to 4 by addition of 1N aqueous NaOH, and the aqueous layer was extracted twice with EtOAc. The organic layer was dried over MgSO4, filtered and adsorbed on silica gel. Purification on silica gel with a gradient of EtOAc/hexanes afforded (5-bromo-1H-pyrrolo[2,3-b]pyridine-3-yl)-phenyl-methanone as a white solid (61 mg, 40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361763B2
Source datasetuspto-grants-2008_04
ORD IDord-db4582f2b8474f6d954bd1e1ae16d4a8
Source noteuspto-grants-2008_04