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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067514Generated: November 3, 2026

Sodium hydride → HCID 22989380, compound

https://huagongshe.com/reaction/1067514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
ReactantHCID 22989220HCID 22989220—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22989380HCID 22989380145.7%

Reaction Steps

210 mg of 60% sodium hydride in oil was suspended in 15 ml of tetrahydrofuran; 0.91 g of 4-(diphenylmethyl)-1-piperazinehexanol was added, followed by heating and refluxing for 1 hour. After cooling, 440 mg of 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine was added, followed by heating and refluxing for 3 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; 1.44 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 1.06 g of the title compound, which was then recrystallized from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-5a27d4620f914c449e6327ba404951e2
Source noteuspto-grants-2001_06