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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626000Generated: November 2, 2026

Methyl Ethyl Ketone → 5-Bromo-2,3-dimethyl-1H-pyrrolo[2,3-B]pyridine

https://huagongshe.com/reaction/1626000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
Reactant5-Bromo-2-hydrazinopyridineHCID 11535699—
SolventEthanolHCID 702—
Product5-Bromo-2,3-dimethyl-1H-pyrrolo[2,3-B]pyridineHCID 19392612—

Reaction Steps

2-Butanone (715 μl) was added to a solution of 5-bromo-2-hydrazinopyridine (1000 mg) in ethanol (10 ml), and the mixture was heated under reflux for 2 hours. The reaction solution was concentrated under reduced pressure. Diethylene glycol (10 ml) was added and the mixture was heated under reflux for 23 hours. The reaction solution was concentrated under reduced pressure and separated by adding dichloromethane and distilled water. The resulting organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (developed with methanol-chloroform) to give the title compound (104 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785438B2
Source datasetuspto-grants-2014_07
ORD IDord-96bf4b51a7b94dce8409902f14a78f41
Source noteuspto-grants-2014_07