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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69223Generated: October 25, 2026

Ethyl Acetate → (Rac)-2-(4-{3-[1-(5,7-difluoro-quinolin-6-yl)-ethyl]-imidazo[1,2-b]pyridazin-6-yl}-pyrazol-1-yl)ethanol

https://huagongshe.com/reaction/69223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant(Rac)-6-[1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-ethyl]-5,7-difluoro-quinolineHCID 58147541—
Reactant1-[2-(oxan-2-yloxy)ethyl]-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 59341819—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(Rac)-2-(4-{3-[1-(5,7-difluoro-quinolin-6-yl)-ethyl]-imidazo[1,2-b]pyridazin-6-yl}-pyrazol-1-yl)ethanolHCID 57917349—

Reaction Conditions

Temperature150 °C

Reaction Steps

(rac)-6-[1-(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-ethyl]-5,7-difluoro-quinoline (Stage 182.1, 620 mg, 1.529 mmol) was dissolved in DME (5 mL) in a microwave reactor with 1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (Stage 171.4, 493 mg, 1.529 mmol) and a solution of 2 M Na2CO3 (2.75 mL). Then tetrakis(triphenylphosphine)-palladium (88 mg) was added and the RM was heated at 150° C. for 15 min under microwave irradiations. It was then taken up with EtOAc and washed with 10% Na2CO3 sol. and brine. The organic layer was dried over Na2SO4 and the solvent was removed. It was then dissolved in DCM (18 mL) and HCl in dioxane (4 N, 1.146 mL) was added. It was stirred at rt for 2 h. The solvent was removed and it was taken up in EtOAc/MeOH (9:1) and washed with water and brine. The organic layer was dried over Na2SO4 and the solvent was removed. The residue was triturated with Et2O and the solid was filtered off. The yellow solid obtained was the pure racemate of the title compound (tR 1.1 min (conditions 2), MH+=421)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-7fd314cde442447d832db07e53715aea
Source noteuspto-grants-2014_09