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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279072Generated: October 29, 2026

Cesium fluoride → 3-Bromo-N-[(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]imidazo[1,2-b]pyridazin-6-amine

https://huagongshe.com/reaction/2279072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
Reactant(S)-1-(5-Fluoropyrimidin-2-YL)ethanamineHCID 55285341—
SolventDimethyl SulfoxideHCID 679—
Product3-Bromo-N-[(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]imidazo[1,2-b]pyridazin-6-amineHCID 8670232864%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 3-bromo-6-chloroimidazo[1,2-b]pyridazine (Preparation 1b, 0.2 g, 0.86 mmol), (1S)-1-(5-fluoropyrimidin-2-yl)ethanamine (prepared according to the method described in WO2006/82392A1, 0.24 g, 1.72 mmol), cesium fluoride (1.31 g, 8.60 mmol) and dimethylsulfoxide (5 mL) was heated at 180° C. for 2 hours in a sealed tube. The reaction was cooled down, filtered through Celite® eluting with ethyl acetate and the filtrate was washed with water, dried over magnesium sulphate and the solvent removed under reduced pressure. The residue was purified by flash chromatography (40-70% acetone in hexanes) to give the title compound (0.11 g, 64%) as a brown foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133200B2
Source datasetuspto-grants-2015_09
ORD IDord-928e98ec59834057bfd4880bf1bfd7e5
Source noteuspto-grants-2015_09