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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383308Generated: October 30, 2026

Chloroacetaldehyde → 6-Chloroimidazo(1,2-a)pyridine

https://huagongshe.com/reaction/383308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantEthanolHCID 702—
Reactant5-Amino-2-chloropyridineHCID 79305—
Product6-Chloroimidazo(1,2-a)pyridineHCID 2764328—

Reaction Steps

To a solution of 50% aq. chloroacetaldehyde (1.1 eq, 291 mmol, 37 ml) in ethanol (700 ml) is added 3-amino-6-chloro-pyridine (1 eq, 264 mmol, 34 g) at room temperature. The reaction mixture is refluxed for 3 hours. The solvent is removed in vacuo and the crude product is dissolved in water (400 ml). The aqueous solution is treated with sodium bicarbonate to pH=8 and extracted with dcm (3×250 ml), the organic layer is dried (MgSO4) and evaporated to give a brown solid (39.2 g) 6-chloro-imidazo[1,2-a]pyridine; [M+H]+153(155)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367662B2
Source datasetuspto-grants-2013_02
ORD IDord-9e04716f52c14a95aa5b45a01dacfbd8
Source noteuspto-grants-2013_02