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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69250Generated: October 29, 2026

Hydrochloric Acid → HCID 57917286, compound

https://huagongshe.com/reaction/69250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylamineHCID 6341—
ReactantSodium HydroxideHCID 14798—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Quinolin-6-ylmethyl-imidazo[1,2-b]pyridazine-6-carbonitrileHCID 57917322—
SolventMethanolHCID 887—
ProductHCID 57917286HCID 57917286—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Quinolin-6-ylmethyl-imidazo[1,2-b]pyridazine-6-carbonitrile (Example 208; 43 mg, 0.15 mmol) in a 1 M aqueous solution of NaOH (1.8 mL, 1.8 mmol) was heated under microwave irradiation at 200° C. for 30 min. The RM was quenched with a 2 M aqueous solution of HCl (0.9 mL, 1.8 mmol) and diluted with MeOH and filtered over Celite. The filtrate is evaporated and dry under vacuo. The residue was suspended in DCM (3 mL) and cooled at 0° C. Were added DMF (0.01 mL) and, slowly, oxalyl chloride (0.055 mL, 0.65 mmol). The RM was allowed to reach rt and stirred at this temperature for 45 min. The RM was dropped in a 2 M solution of ethylamine in MeOH (6 mL). The RM was stirred at rt for 5 min before being evaporated to dryness and the residue quenched with aqueous saturated NaHCO3 and diluted with EtOAc. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine and dried over Na2SO4, filtered and evaporated. The residue was purified by preparative HPLC with acetonitrile and water (+0.1% TFA) to yield the title compound as light yellow solid (tR 1.96 min (conditions 8), MH+=332).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822468B2
Source datasetuspto-grants-2014_09
ORD IDord-88f46a0a2fbe495ba902909707641450
Source noteuspto-grants-2014_09