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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067523Generated: November 2, 2026

Dimethylformamide → Ethyl 6-[3-[4-(Diphenylmethoxy)piperidino]propylamino]imidazo[1,2-b]pyridazine-2-carboxylate Difumarate

https://huagongshe.com/reaction/1067523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactantethyl 6-chloroimidazo[1,2-b]pyridazine-2-carboxylateHCID 2779714—
Reactant4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
ProductEthyl 6-[3-[4-(Diphenylmethoxy)piperidino]propylamino]imidazo[1,2-b]pyridazine-2-carboxylate DifumarateHCID 69843796—

Reaction Conditions

Temperature80 °C

Reaction Steps

686 mg of 4-(diphenylmethoxy)-1-piperidinepropanamine and 477 mg of ethyl 6-chloroimidazo[1,2-b]pyridazin-2-carboxylate were dissolved in 7 ml of N,N-dimethylformamide; 0.73 ml of N-ethyldiisopropylamine was added, followed by stirring in an oil bath (80° C.) for 18.5 hours. After cooling, ice water and saline were added, followed by extraction with ethyl acetate-tetrahydrofuran (1:1); the extract was washed with saturated saline and dried with magnesium sulfate. The dry product was 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, dissolved in 5 ml of ethyl acetate; a solution of 95 mg of fumaric acid in 5 ml of ethanol was added, followed by concentration. Acetone-ethyl ether (1:2) was added to the residue to cause recrystallization; the crystal precipitate was collected by filtration and washed with ethyl ether to yield 211 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-fa3f0acf4aad47a380bac183c5d8e58c
Source noteuspto-grants-2001_06