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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539731Generated: October 26, 2026

6-Methoxypyridazin-3-amine → 6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/539731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxypyridazin-3-amineHCID 81673—
Reactant2-Bromo-1-(4-methyl-3-nitrophenyl)ethan-1-oneHCID 3800422—
SolventAcetonitrileHCID 6342—
Product6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 6808915585.2%

Reaction Steps

A stirred solution of 6-methoxypyridazin-3-amine (Apollo Scientific, 0.750 g, 5.99 mmol) and 2-bromo-1-(4-methyl-3-nitrophenyl)ethanone (1.54 g, 5.99 mmol) in acetonitrile (20 mL) is heated at 80° C. for 16 hours. The reaction mixture is concentrated to dryness and purified via chromatography (hexanes to EtOAc) to afford the title compound (1.45 g, 85%) as a light yellow solid: Rf 0.45 (1:1 EtOAc:hexanes); LCMS (m/z)=285.4 [M+H]+, tR=7.47 min. (10 min run)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871767B2
Source datasetuspto-grants-2014_10
ORD IDord-0bd679a3722445f3b5d6d8b99bb02dc5
Source noteuspto-grants-2014_10