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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067586Generated: November 1, 2026

Methyl iodide → 6-Chloro-2-methoxyimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1067586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-Chloroimidazo[1,2-b]pyridazin-2-olHCID 22989329—
SolventDimethylformamideHCID 6228—
Product6-Chloro-2-methoxyimidazo[1,2-b]pyridazineHCID 22989338—

Reaction Steps

2.69 g of 6-chloro-2-hydroxyimidazo[1,2-b]pyridazine was suspended in 30 ml of N,N-dimethylformamide; 838 mg of a 60% sodium hydride dispersion in mineral oil was added little by little, followed by stirring at room temperature for 30 minutes. Under ice water cooling conditions, 1.2 ml of methyl iodide was added, followed by stirring at room temperature for 3 days. Ice water was added, followed by extraction with ethyl acetate; the extract was washed with saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with hexane:ethyl acetate (5:1). The desired fraction was collected and concentrated to yield 1.05 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-ffcf693d184b444e8fcd9a2c420dd100
Source noteuspto-grants-2001_06