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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067500Generated: October 27, 2026

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

https://huagongshe.com/reaction/1067500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
Reactant6-Chloro-2-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 12212526—
Solvent1-ButanolHCID 263—
SolventEthyl AcetateHCID 8857—
Product6-[3-[4-(Diphenylmethoxy)piperidino]propylamino]-2-methyl[1,2,4]triazolo[1,5-b]pyridazineHCID 1103781630.9%

Reaction Steps

6-Chloro-2-methyl[1,2,4]triazolo[1,5-b]pyridazine (655 mg) and 4-(diphenylmethoxy)-1-piperidinepropanamine (1.26 g) was suspended in n-butanol (20 ml), followed by addition of N-ethyldiisopropylamine (1.94 ml). The mixture was refluxed under heating for 22 hours, followed by addition of ice-water and sodium hydrogen carbonate and extraction with ethyl acetate. The extract was washed with an aqueous sodium chloride saturated solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica-gel column chromatography and eluted with a mixture of ethyl acetate, methanol and triethylamine (50:5:1). Fractions containing the objective compound were collected and concentrated. The resulting crystals were washed with hexane and dried to yield the title compound (547 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-ac804332a42d45d58959d9725f7690ea
Source noteuspto-grants-2001_06