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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096306Generated: October 27, 2026

1-Butanol → 6-(2-(3-Fluorophenyl)piperidin-1-yl)-3-nitroimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/2096306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Fluorophenyl)piperidineHCID 4360128—
Reactant6-Chloro-3-nitro-imidazo(1,2-b)pyridazineHCID 10535981—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product6-(2-(3-Fluorophenyl)piperidin-1-yl)-3-nitroimidazo[1,2-b]pyridazineHCID 67307668—

Reaction Conditions

Temperature180 °C

Reaction Steps

To a pressure reaction tube were charged 6-chloro-3-nitroimidazo[1,2-b]pyridazine (450 mg, 2.27 mmol), 2-(3-fluorophenyl)piperidine (609 mg, 3.40 mmol, purchased from ChemBridge), and N-ethyl-N-isopropylpropan-2-amine (0.51 mL, 2.95 mmol), followed by addition of 1.0 mL n-butanol. The reaction mixture was then sealed and stirred at 180° C. for 24 hours. After completion, the reaction was cooled to ambient temperature, and diluted with water and EtOAc. The organic layer was separated, and the aqueous layer was extracted with EtOAc twice. The combined organic layers was dried over Na2SO4 and concentrated. The crude product was purified by silica column chromatography, eluting with 20 to 50% EtOAc in hexanes to yield the desired product for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450322B2
Source datasetuspto-grants-2013_05
ORD IDord-2e1a11a8ad66481ebea9cc12a070e497
Source noteuspto-grants-2013_05