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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879390Generated: October 31, 2026

6-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde → 6-bromo-3-methyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/879390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 18400665—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product6-bromo-3-methyl-1H-pyrrolo[2,3-b]pyridineHCID 58086543—

Reaction Steps

LAH (1.0M in THF, 4.45 mL, 4.45 mmol) was added dropwise to refluxing 6-bromo-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (1000 mg, 4.45 mmol) in dry THF (16 mL). The mixture was refluxed for 1 h, allowed to attain room temperature, and quenched with water (0.34 mL), w/w 15% aq. NaOH (0.34 mL) and water (1 mL). The resulting precipitation was filtered off, the filtrate concentrated and the residue was partitioned between aqueous NaOH and DCM. The organic layers were combined, dried and concentrated to give title compound. LCMS-ESI+: calc'd for C8H7BrN2: 211.2 (M+H+); Found: 211.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-87e40ba6e25749b0a484ed8411730d26
Source noteuspto-grants-2015_03