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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969102Generated: October 31, 2026

2-Aminopyridine → HCID 57786669, compound

https://huagongshe.com/reaction/1969102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantSodium hydrideHCID 24758—
Reactant6,8-Dichloroimidazo[1,2-b]pyridazineHCID 57517539—
SolventDimethylformamideHCID 6228—
ProductHCID 57786669HCID 5778666935%

Reaction Steps

A solution of 2-aminopyridine (0.388 g, 4.12 mmol) in 8 mL of N,N-dimethylformamide was treated with 60% sodium hydride/mineral oil (0.167 g, 4.18 mmol) and the lightly bubbling, pale yellow solution was stirred for 30 min., in which time it became a dark yellow cloudy solution. The solution was added via Pasteur pipette to a flask containing 6,8-dichloro-imidazo[1,2-b]pyridazine (0.310 g, 1.65 mmol), and the cloudy orange solution was stirred for 16 h then partitioned between 80 mL of a saturated aq. NH4Cl solution and 80 mL of ether. The organic layer was sequentially washed with two 40 mL portions of water and 40 mL of a saturated aq. NaCl solution; dried over MgSO4, filtered and concentrated to a pale yellow solid. Column chromatography (0->33% EtOAc/hexanes) afforded 0.141 g (35%) of (6-chloro-imidazo[1,2-b]pyridazin-8-yl)-pyridin-2-yl-amine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426441B2
Source datasetuspto-grants-2013_04
ORD IDord-552038548e9a4dd5b006d0bd11a6733b
Source noteuspto-grants-2013_04