Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896355Generated: October 30, 2026

6-Amino-3-chloropyridazine → 6-Chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1896355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3-chloropyridazineHCID 21643—
Reactant3-Bromo-1,1,1-trifluorobutan-2-oneHCID 2736410—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-Chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazineHCID 53629153—

Reaction Steps

A solution of 6-chloro-3-aminopyridazine x34 (3.16 g, 1 eq, 24.2 mmol) and 3-bromo-1,1,1-trifluorobutan-2-one (5 g, 1 eq, 24.4 mmol) in 1,2-dimethoxyethane (100 ml) is refluxed during 17 hours. After cooling to room temperature and filtration, the solvent is removed under reduced pressure and the crude mixture is purified by preparative chromatography on silicagel (CH2Cl2/MeOH/NH4OH: 98/2/0.2 (v/v/v)) leading to 6-chloro-3-methyl-2-(trifluoromethyl)imidazo[1,2-b]pyridazine x35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518943B2
Source datasetuspto-grants-2013_08
ORD IDord-a836f299d7d346d0a3cf1a48d08a7d4c
Source noteuspto-grants-2013_08