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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846002Generated: October 31, 2026

Sodium Carbonate → 7-Ethyl-4-(4-fluorophenyl)-7H-imidazo[4,5-c]pyridazine

https://huagongshe.com/reaction/1846002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant4-chloro-7-ethyl-7H-imidazo(4,5-c)pyridazineHCID 55296765—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product7-Ethyl-4-(4-fluorophenyl)-7H-imidazo[4,5-c]pyridazineHCID 8672323155%

Reaction Steps

To a room temperature solution of 4-chloro-7-ethyl-7H-imidazo[4,5-c]pyridazine (Preparation 8, 9.6 g, 52.4 mmol) in dioxane (300 mL) was added 4-fluorobenzene boronic acid (8.8 g, 63 mmol) and an aqueous solution of Na2CO3 (1M, 260 mL, 262 mmol). The reaction mixture was degassed and purged with nitrogen gas 3 times. Tetrakis(triphenylphosphine)palladium(0) (1.2 g, 1.0 mmol) was then added and the mixture was heated to reflux for 4 hours. The organic solvent was removed in vacuo and the resulting aqueous mixture filtered. The filter cake was dried under vacuum to afford the title compound as a yellow solid in 55% yield, 7 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952008B2
Source datasetuspto-grants-2015_02
ORD IDord-96a4e5224f8f4056a293796670b78022
Source noteuspto-grants-2015_02