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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169037Generated: November 1, 2026

Diisopropylethylamine → 6-[3-[4-(Diphenylmethoxy)piperidino]propylamino]-2-phenyl[1,2,4]triazolo[1,5-b]pyridazine

https://huagongshe.com/reaction/1169037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Chloro-2-phenyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 1459119—
Reactant4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
Solvent1-ButanolHCID 263—
Product6-[3-[4-(Diphenylmethoxy)piperidino]propylamino]-2-phenyl[1,2,4]triazolo[1,5-b]pyridazineHCID 2298931637.6%

Reaction Steps

365 mg of 6-chloro-2-phenyl[1,2,4]triazolo[1,5-b]pyridazine and 0.513 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 8 ml of 1-butanol; 0.54 ml of N-ethyldiisopropylamine was added, followed by heating and refluxing for 19 hours. Ice water and sodium hydrogen carbonate were added, followed by extraction with ethyl acetate; the extract was washed with saturated saline, dried over magnesium sulfate and 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 and concentrated; the resulting crystal was recrystallized from ethyl acetate to yield 308 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627630B1
Source datasetuspto-grants-2003_09
ORD IDord-fcdd091e088a4c8c962258da02ec77d4
Source noteuspto-grants-2003_09