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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169070Generated: October 26, 2026

Sodium Bicarbonate → 2-[6-[4-[4-(Diphenylmethoxy)piperidino]butylamino]imidazo[1,2-b]pyridazin-2-yl]-2-methylpropionic Acid

https://huagongshe.com/reaction/1169070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-(6-chloroimidazo[1,2-b]pyridazin-2-yl)-2-methylpropanoateHCID 11043751—
Reactant1-Piperidinebutanamine, 4-(diphenylmethoxy)-HCID 11739259—
Product2-[6-[4-[4-(Diphenylmethoxy)piperidino]butylamino]imidazo[1,2-b]pyridazin-2-yl]-2-methylpropionic AcidHCID 2298926321.7%

Reaction Steps

1.56 g of 4-(diphenylmethoxy)-1-piperidinebutanamine and 617 mg of ethyl 2-(6-chloroimidazo[1,2-b]pyridazin-2-yl)-2-methylpropionate were stirred at 185° C. for 3 hours. After cooling, aqueous sodium bicarbonate was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol:triethylamine (50:5:1). The desired fraction was collected, concentrated under reduced pressure and dissolved in 5 ml of ethyl acetate; 0.52 ml of a 4 N hydrogen chloride solution in ethyl acetate was added, followed by concentration. The residue was dissolved in 4 ml of ethanol; 4 ml of a 1 N aqueous solution of sodium hydroxide was added, followed by stirring at room temperature for 4 hours; 1 ml of a 2 N aqueous solution of sodium hydroxide was added, followed by stirring at 50° C. for 16 hours. The mixture was concentrated under reduced pressure. The residue was diluted with water and washed with ethyl acetate; the water layer was adjusted to pH 4.5 by the addition of 4 N hydrochloric acid and extracted with ethyl acetate-tetrahydrofuran (1:1); the extract was washed with saturated saline, dried over magnesium sulfate and concentrated under reduced pressure. The residue was powdered by the addition of ethyl acetate, collected by filtration and dried to yield 271 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627630B1
Source datasetuspto-grants-2003_09
ORD IDord-1598175b8fc54b56b2d28f3f566fb7b4
Source noteuspto-grants-2003_09