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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279063Generated: October 30, 2026

Dichloromethane → HCID 86702325, compound

https://huagongshe.com/reaction/2279063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactant(2-Methoxypyridin-3-yl)boronic acidHCID 2762709—
Reactant3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86702325HCID 8670232562.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-bromo-6-chloroimidazo[1,2-b]pyridazine (Preparation 1b, 6.0 g, 25.81 mmol), (2-methoxypyridin-3-yl)boronic acid (3.3 g, 21.58 mmol), cesium carbonate (30 mL of a 2M solution in water, 60 mmol) and 1,4-dioxane (250 mL) in a Schlenk vial was subjected to three cycles of evacuation backfilling with argon. [1,1′-Bis(diphenyl phosphino)ferrocene]-dichloropalladium(II) complex with dichloromethane (1:1) (1.8 g, 2.16 mmol) was then added and the resulting mixture was again subjected to three further cycles of evacuation backfilling before being heated at 100° C. for 2 hours. Subsequently, the reaction was cooled down, diluted with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulphate and the solvent removed under reduced pressure. The residue was treated with ethyl acetate and the solid formed was filtered, washed with dichloromethane and dried in vacuo to yield the title compound (3.5 g, 62%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133200B2
Source datasetuspto-grants-2015_09
ORD IDord-9b319f63980f4548b22bd106e6415835
Source noteuspto-grants-2015_09