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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239852Generated: October 31, 2026

6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amine → HCID 178511634, compound

https://huagongshe.com/reaction/2239852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amineHCID 86611730—
ReactantHCID 178511674HCID 178511674—
SolventWaterHCID 962—
ProductHCID 178511634HCID 178511634—

Reaction Steps

In a 2 dram reaction vial was added crude 6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amine (0.42 g, 1.4 mmol) from 1a and trans-1,4-diaminocyclohexane (1.0 g, 8.0 mmol). The mixture was allowed to melt at 160° C. for 8 hrs. The melt was then cooled, diluted with water and extracted with dichloromethane. The organic layer was concentrated to provide crude N6-((trans)-4-aminocyclohexyl)-N8-(4-nitrophenyl)imidazo[1,2-b]pyridazine-6,8-diamine which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-995372ea6b4a41dd958deb000c2d19ea
Source noteuspto-grants-2010_05