Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239823Generated: November 2, 2026

Chloroacetaldehyde → 8-bromo-6-chloro-7-methylimidazo[1,2-b]pyridazine HCl salt

https://huagongshe.com/reaction/2239823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant4-Bromo-6-chloro-5-methylpyridazin-3-amineHCID 59624331—
SolventEthanolHCID 702—
Product8-bromo-6-chloro-7-methylimidazo[1,2-b]pyridazine HCl saltHCID 8661171390%

Reaction Conditions

Temperature110 °C

Reaction Steps

Chloroacetaldehyde (1.6 ml, 10 mmol, 50% in H2O) was added to a solution of crude 4-bromo-6-chloro-5-methylpyridazin-3-amine (0.5 g, 2 mmol) from 1b in EtOH (5 mL). The mixture was heated in a sealed vial at 110° C. for 2 h. Solvent was removed in vacuo and the resulting solid was suspended in acetone/Et2O (1/1, 5 mL), filtered, and then washed with Et2O to give 8-bromo-6-chloro-7-methylimidazo[1,2-b]pyridazine HCl salt (0.5 g, >90% pure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-a992115143d74a6aae712d2ca0ba2785
Source noteuspto-grants-2010_05