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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945604Generated: October 30, 2026

Chloroacetaldehyde → 8-(Benzyloxy)-5-bromoimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1945604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant3-(Benzyloxy)-6-bromopyridin-2-amineHCID 59605512—
Product8-(Benzyloxy)-5-bromoimidazo[1,2-a]pyridineHCID 5960526188%

Reaction Steps

A mixture of 3-benzyloxy-6-bromopyridin-2-ylamine (1.0 g, 3.6 mmol) and chloroacetaldehyde (1.2 mL, 50 wt. % in water) in IMS (12 mL) was stirred at reflux for 1 hour, then concentrated under reduced pressure. The residue was partitioned between an aqueous saturated solution of sodium bicarbonate and EtOAc. The organic layer was separated and washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (Si—PPC, MeOH:Et2O, gradient 0:100 to 1:99) to give 8-Benzyloxy-5-bromo-imidazo[1,2-a]pyridine as an beige solid (960 mg, 88%). LCMS (Method H) RT 3.08 min; [M+H]+ 303 (79Br) and 305 (81Br)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-e439b2e1677841ddb63b3c820eeadb2c
Source noteuspto-grants-2013_03