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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539735Generated: October 25, 2026

Chlorosuccinimide → 3-Chloro-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/539735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 68089155—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product3-Chloro-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 6808912298.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine (0.250 g, 0.879 mmol) in acetonitrile (20 mL) is added N-chlorosuccinimide (0.879 mmol) and the mixture is heated at 60° C. for 8 hours. The reaction mixture is diluted with water (50 mL), and sat. aqueous NaHCO3 (50 mL). The precipitate that forms is collected by filtration, washed with water (3×25 mL) and dried under vacuum to give the title compound (0.277 g, 98% yield) as a yellow solid: Rf 0.60 (1:1 EtOAc:hexanes); LCMS (m/z)=319.3, 321.2 [M+H]+, tR=3.02 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871767B2
Source datasetuspto-grants-2014_10
ORD IDord-4060c1a9e1d94f638fa118f7ad383a98
Source noteuspto-grants-2014_10