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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067512Generated: October 26, 2026

Sodium hydride → 6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy] ethoxy][1,2,4]triazolo[1,5-b]pyridazine dihydrochloride

https://huagongshe.com/reaction/1067512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDecloxizineHCID 71135—
Reactant6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
SolventTetrahydrofuranHCID 8028—
Product6-[2-[2-[4-(Diphenylmethyl)piperazino]ethoxy] ethoxy][1,2,4]triazolo[1,5-b]pyridazine dihydrochlorideHCID 22989414157%

Reaction Steps

100 mg of 60% sodium hydride in oil was suspended in 20 ml of tetrahydrofuran; 470 mg of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine was added, followed by heating and refluxing for 1 hour. After cooling, 200 mg of 6-chloro[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 4.5 hours. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saturated saline and dried with magnesium sulfate. After the dry product was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with dichloromethane-ethyl acetate-methanol (10:10:1). The desired fraction was collected and dissolved in 5 ml of ethyl acetate; 0.83 ml of a 4 N hydrogen chloride solution in ethyl acetate was added; the crystal precipitated was collected by filtration, washed with ethyl ether and dried to yield 0.54 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-d09406e9a40245e086862f96d16a6045
Source noteuspto-grants-2001_06