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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69248Generated: October 29, 2026

N-methyl-2-pyrrolidone → 3-Quinolin-6-ylmethyl-imidazo[1,2-b]pyridazine-6-carbonitrile

https://huagongshe.com/reaction/69248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-quinolineHCID 44206294—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
Product3-Quinolin-6-ylmethyl-imidazo[1,2-b]pyridazine-6-carbonitrileHCID 57917322—

Reaction Steps

(6-Chloro-imidazo[1,2-b]pyridazin-3-yl)-quinoline (Example 14) (50 mg, 0.17 mmol) and CuCN (23 mg, 0.26 mmol) in 0.5 mL NMP were heated under microwave irradiation at 230° C. for 9.5 h. The RM was diluted with EtOAc and washed with aqueous saturated NaHCO3 and brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by preparative HPLC with acetonitrile and water (+0.1% TFA) to yield the title compound as a yellow solid (tR 2.16 min (conditions 8), MH+=286).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-e5b9edf2872c43308c805818c8337249
Source noteuspto-grants-2014_09