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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69210Generated: October 26, 2026

1,2-Dimethoxyethane → 5,7-Difluoro-6-(6-{1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-pyrazol-4-yl}-imidazo[1,2-b]pyridazin-3-ylmethyl)-quinoline

https://huagongshe.com/reaction/69210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-5,7-difluoro-quinolineHCID 58147526—
Reactant1-[2-(oxan-2-yloxy)ethyl]-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 59341819—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthyl AcetateHCID 8857—
Product5,7-Difluoro-6-(6-{1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-pyrazol-4-yl}-imidazo[1,2-b]pyridazin-3-ylmethyl)-quinolineHCID 68634255—

Reaction Conditions

Temperature150 °C

Reaction Steps

6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-5,7-difluoro-quinoline (Stage 171.2, 90 mg, 0.272 mmol) was introduced in a microwave reactor together 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, 88 mg, 0.272 mmol), tetrakis-(triphenylphosphine)-palladium (15.72 mg), 2 M Na2CO3 (0.490 mL) and DME (0.9 mL). The mixture was heated at 150° C. under microwave irradiation for 30 min. The RM was taken up with EtOAc and washed with 10% Na2CO3 and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was dissolved in MeOH and filtered through a cartridge of PL-Thiol to remove the palladium. The filtrate was then purified by preparative HPLC with acetonitrile and water (+0.1% TFA) to afford the title compound (tR 1.1 min (conditions 2), MH+=491).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-8408c0714f0d43c98a75e8d03c30f219
Source noteuspto-grants-2014_09