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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176621Generated: October 26, 2026

Water → (6-Phenylimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone

https://huagongshe.com/reaction/2176621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant1,4-DioxaneHCID 31275—
ReactantPhenylboronic AcidHCID 66827—
Reactant(6-Chloroimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanoneHCID 86630275—
CatalystPalladium ChlorideHCID 24290—
CatalystHCID 178478483HCID 178478483—
Product(6-Phenylimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanoneHCID 67502844—

Reaction Steps

A 48 mL sealed tube was charged with (6-chloroimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone (0.530 g, 1.72 mmol), phenylboronic acid (0.314 g, 2.58 mmol), cesium carbonate (1.68 g, 5.15 mmol), PdCl2(dppf-CH2Cl2 adduct (0.0701 g, 0.0858 mmol), 1,4-dioxane (6.31 ml, 73.8 mmol), and water (1.11 ml, 61.8 mmol), flushed with argon, sealed, then placed in an 80° C. oil bath for 8 hours. The mixture was concentrated then triturated with water, followed by MeOH/DCM to give (6-phenylimidazo[1,2-b]pyridazin-3-yl)(quinolin-6-yl)methanone as a reddish brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066954B2
Source datasetuspto-grants-2015_06
ORD IDord-780d2d194e214c1696c6a36cc85ac3ba
Source noteuspto-grants-2015_06