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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483838Generated: November 1, 2026

Potassium Fluoride → 4-((3-(3-Chlorophenyl)imidazo[1,2-b]pyridazin-6-yl)amino)cyclohexane-1-sulfonamide

https://huagongshe.com/reaction/1483838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant6-Chloro-3-(3-chlorophenyl)imidazo[1,2-b]pyridazineHCID 57418686—
Reactant4-Aminocyclohexane-1-sulfonamideHCID 89389897—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product4-((3-(3-Chlorophenyl)imidazo[1,2-b]pyridazin-6-yl)amino)cyclohexane-1-sulfonamideHCID 71235300—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4-aminocyclohexane-1-sulfonamide (200 mg, 1.12 mmol), 6-chloro-3-(3-chlorophenyl)imidazo[1,2-b]pyridazine (200 mg, 0.76 mmol) and KF (500 mg, 8.6 mmol) in DMSO (2 mL) was heated at 120° C. overnight. LCMS showed the reaction was complete. The mixture was poured into brine (80 mL) and extracted with EtOAc (30 mL×3). The combined extracts were dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by to prep. HPLC give two isomers: EX. 8-81 isomer 1 (7.0 mg) and EX. 8-81 isomer 2 (8.1 mg) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416132B2
Source datasetuspto-grants-2016_08
ORD IDord-3cd0fb73d6e44b369387cef95200a08f
Source noteuspto-grants-2016_08