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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067515Generated: October 25, 2026

Sodium hydride → 6-[6-[4-(Diphenylmethoxy)piperidino]hexyloxy]-7-methyl[1,2,4]triazolo[1,5-b]pyridazine Hydrochloride

https://huagongshe.com/reaction/1067515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
Reactant4-(Diphenylmethoxy)-1-piperidinehexanolHCID 22989378—
SolventTetrahydrofuranHCID 8028—
Product6-[6-[4-(Diphenylmethoxy)piperidino]hexyloxy]-7-methyl[1,2,4]triazolo[1,5-b]pyridazine HydrochlorideHCID 2298943238.7%

Reaction Steps

160 mg of 60% sodium hydride in oil was suspended in 20 ml of tetrahydrofuran; 1.24 g of 4-(diphenylmethoxy)-1-piperidinehexanol was added, followed by heating and refluxing for 1 hour. After cooling, 570 mg of 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 1 hour. 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 and dissolved in 5 ml of ethyl acetate; 0.54 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 0.70 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-34b382ab411a44218eb65afaaefd94be
Source noteuspto-grants-2001_06