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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067596Generated: October 25, 2026

Water → N-(6-chloroimidazo[1,2-b]pyridazine-2-carbonyl)-2,2-dimethylglycine ethyl ester

https://huagongshe.com/reaction/1067596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acidHCID 2794637—
ReactantEthyl 2-amino-2-methylpropanoate hydrochlorideHCID 22343822—
SolventDimethylformamideHCID 6228—
ProductN-(6-chloroimidazo[1,2-b]pyridazine-2-carbonyl)-2,2-dimethylglycine ethyl esterHCID 2298935759.6%

Reaction Steps

1.28 g of 6-chloroimidazo[1,2-b]pyridazine-2-carboxylic acid was suspended in 12 ml of N,N-dimethylformamide; 1.16 g of N,N′-carbonyldiimidazole was added, followed by stirring at room temperature for 30 minutes. To the reaction mixture, 1.20 g of 2-aminoisobutyric acid ethyl ester hydrochloride and 1.00 ml of triethylamine were added, followed by stirring at room temperature for 16 hours. Water was added, the crystal precipitated was collected by filtration; the filtrate was extracted with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; the residue was combined with the above crystal collected by filtration and subjected to silica gel column chromatography and eluted with hexane:ethyl acetate (2:1). The desired fraction was collected and concentrated under reduced pressure to yield 1.20 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-cdc95240a6dd4e28b54fac4a951b4ad1
Source noteuspto-grants-2001_06