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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943462Generated: October 26, 2026

6-chloro-N-(3-fluoropyridin-4-yl)-8-(isoxazol-3-ylamino)imidazo[1,2-b]pyridazine-3-carboxamide → HCID 178511637, compound

https://huagongshe.com/reaction/1943462

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(3-fluoropyridin-4-yl)-8-(isoxazol-3-ylamino)imidazo[1,2-b]pyridazine-3-carboxamideHCID 59624780—
ReactantHCID 178511674HCID 178511674—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178511637HCID 17851163776.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 6-chloro-N-(3-fluoropyridin-4-yl)-8-(isoxazol-3-ylamino)imidazo[1,2-b]pyridazine-3-carboxamide (20 mg, 0.054 mmol) and trans-cyclohexane-1,4-diamine (61.1 mg, 0.535 mmol) in NMP (0.4 mL) was heated at 110° C. overnight, then cooled to room temperature. The resulting mixture was purified by reversed-phase preparative HPLC. The desired fractions were concentrated and dried to give 18.7 mg of 6-((trans-4-aminocyclohexyl)amino)-N-(3-fluoro-4-pyridinyl)-8-(3-isoxazolylamino)imidazo[1,2-b]pyridazine-3-carboxamide as a beige solid. HPLC Rt=2.292 min (Chromolith SpeedROD 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA, 4 min gradient, monitored at 220 nm), [M+1]=452.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389527B2
Source datasetuspto-grants-2013_03
ORD IDord-64e1a7b60b0240f5a640595d7affc82a
Source noteuspto-grants-2013_03