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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241017Generated: October 25, 2026

Formic Acid → 6-Bromo-4H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/241017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
Reactant5-Bromopyridine-2,3-diamineHCID 691156—
Product6-Bromo-4H-imidazo[4,5-b]pyridineHCID 91157895%

Reaction Steps

A suspension of 2,3-diamino-5-bromopyridine (3.0 g, 16.00 mmol) in formic acid (30 mL) was heated to reflux for 3 hours. After cooling the reaction mixture to room temperature it was concentrated and the residue was taken into 50% ethyl acetate in toluene (100 mL) then concentrated and the process repeated once more to remove excess formic acid. The resulting solid was triturated with ethyl acetate and the solid residue collected by filtration to give 6-bromo-1H-imidazo[4,5-b]pyridine (3.7 g, 95%). GCMS (EI) for C6H4BrN3: 198 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-7b5ae499fc8644f7b92cf2b1a9766e7a
Source noteuspto-grants-2014_02