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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162148Generated: November 1, 2026

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

https://huagongshe.com/reaction/1162148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant6-Amino-3-chloropyridazineHCID 21643—
Solvent1-ButanolHCID 263—
ProductImidazo(1,2-b)pyridazine, 6-chloro-HCID 13882852.1%

Reaction Steps

A mixture of 6-chloro-pyridazinamine (5.00 g, 38 mmol) in 1-butanol (5 mL) was treated with chloroacetaldehyde (50% in water, 5.0 mL, 38 mmol) and the tan suspension was refluxed two hours and to give a dark solution. The reaction mixture was cooled to room temperature and the solid was collected by filtration and washed with methanol to afford a brown solid (3.04 g); evaporation of the filtrate gave additional product (4.60 g). The solids were combined (7.64 g) and used in the next reaction without further purification: MS [M+H]+ 154.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820670B2
Source datasetuspto-grants-2010_10
ORD IDord-86bcdbe5ce7d4562956582d2b7f184e0
Source noteuspto-grants-2010_10