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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067519Generated: October 27, 2026

Sodium hydride → 7-t-Butyl-6-[2-[2-[4-(Diphenylmethyl)-1-piperazinyl]ethoxy]ethoxy][1,2,4]triazolo[1,5-b]pyridazine Dihydrochloride

https://huagongshe.com/reaction/1067519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDecloxizineHCID 71135—
Reactant6-Chloro-7-t-butyl[1,2,4]triazolo[1,5-b]pyridazineHCID 22989243—
SolventTetrahydrofuranHCID 8028—
Product7-t-Butyl-6-[2-[2-[4-(Diphenylmethyl)-1-piperazinyl]ethoxy]ethoxy][1,2,4]triazolo[1,5-b]pyridazine DihydrochlorideHCID 22989402171%

Reaction Steps

150 mg of 60% sodium hydride was suspended in 20 ml of tetrahydrofuran; 1.05 g of 4-(diphenylmethyl)-1-[2-(2-hydroxyethoxy)ethyl]piperazine in oil was added, followed by heating and refluxing for 1 hour. After cooling, 650 mg of 6-chloro-7-t-butyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 2 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 ethyl acetate:methanol (10:1). The desired fraction was collected; the residue was dissolved in 5 ml of ethyl acetate; 2.1 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 1.55 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-b182a173a64b4285b6fffd2adf3b9179
Source noteuspto-grants-2001_06