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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539807Generated: October 27, 2026

Potassium Acetate → 2-(4-Methyl-3-nitro-phenyl)-6-[2-(trifluoromethyl)-3-pyridyl]imidazo[2,1-f]pyridazine

https://huagongshe.com/reaction/539807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridineHCID 56924434—
Reactant6-Chloro-2-(4-methyl-3-nitro-phenyl)imidazo[2,1-f]pyridazineHCID 86667857—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Product2-(4-Methyl-3-nitro-phenyl)-6-[2-(trifluoromethyl)-3-pyridyl]imidazo[2,1-f]pyridazineHCID 6808906260%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 500 mL flask is charged with 6-chloro-2-(4-methyl-3-nitro-phenyl)imidazo[2,1-f]pyridazine (10.104 g, 0.035 mol), 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine (Journal of Organic Chemistry, 2011, 76, 1062) (13.38 g, 0.049 mol), KOAc (6.869 g, 0.07 mol), bis(dibenzylideneacetone)palladium(0) (2.01 g, 3.5 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (3.34 g, 0.007 mol), butanol (112 mL) and water (20 mL). The reaction mixture is heated at 90° C. for 4 hr. The reaction is filtered through celite and washed with EtOAc. The liquid layers are combined, concentrated onto celite and purified by silica gel chromatography (0-75% EtOAc in CH2Cl2) to give the title compound (7.98 g, 60% yield). LCMS (m/z)=400.4 [M+H]+, tR=2.76 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871767B2
Source datasetuspto-grants-2014_10
ORD IDord-1cc09979ea154dd3a728a51d1e3b8152
Source noteuspto-grants-2014_10