Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927321Generated: October 30, 2026

Chloroacetaldehyde → Imidazo(1,2-b)pyridazine, 6-chloro-

https://huagongshe.com/reaction/927321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant6-Amino-3-chloropyridazineHCID 21643—
ReactantSodium BicarbonateHCID 516892—
Solvent1-ButanolHCID 263—
ProductImidazo(1,2-b)pyridazine, 6-chloro-HCID 13882870.3%

Reaction Steps

5.0 g (38.6 mmol) of 3-amino-6-chloropyridazine were heated together with 4.7 mL (40 mmol) of chloroacetaldehyde (55% strength in water) in 15 mL of n-butanol at 120° C. for a period of 5 days. After the reaction was complete, the reaction mixture was added to saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The combined organic phases were then washed with brine and dried over sodium sulfate, and the solvent was removed in vacuo. In the final purification by chromatography on silica gel, 4.17 g (70%) of the desired product were isolated in the form of an amorphous white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290482B2
Source datasetuspto-grants-2016_03
ORD IDord-e866de80b9144c598a06d4dcbf80a6f5
Source noteuspto-grants-2016_03