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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222433Generated: November 1, 2026

Hydrochloric Acid → 2-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol

https://huagongshe.com/reaction/2222433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBoron tribromideHCID 25134—
Reactant5-methoxy-2-methyl-1H-pyrrolo[2,3-b]pyridineHCID 22273670—
SolventDichloromethaneHCID 6344—
Product2-methyl-1H-pyrrolo[2,3-b]pyridin-5-olHCID 2227362198.6%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of boron tribromide (64 μl, 0.68 mmol) in methylene chloride (200 μl) was added to a solution of 5-methoxy-2-methyl-1H-pyrrolo[2,3-b]pyridine (50 mg, 0.308 mmol) in methylene chloride (4 ml) cooled at −30° C. The mixture was left to warm up to ambient temperature and further stirred for 3 hours. The mixture was poured onto ice. The pH was adjusted to 6.2 with 6N aqueous sodium hydroxide followed by 2 N aqueous hydrogen chloride. The mixture was extracted with ethyl acetate. The organic layer was washed with water, followed by brine and dried (MgSO4), filtered and the filtrate was evaporated. The residue was purified by column chromatography, eluting with with methylene chloride followed by methylene chloride/methanol (98/2 followed by 95/5). The fractions containing the expected product were combined and evaporated to give 2-methyl-1H-pyrrolo[2,3-b]pyridin-5-ol (45 mg, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371765B2
Source datasetuspto-grants-2008_05
ORD IDord-6e088526f6fb4be38ae52dca7d46a4d7
Source noteuspto-grants-2008_05