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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397556Generated: October 26, 2026

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

https://huagongshe.com/reaction/397556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
Solvent1-ButanolHCID 263—
Product6-[3-(4-(Diphenylmethoxy)piperidino]propylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415048.8%

Reaction Steps

0.464 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine and 1.26 g of 4-(diphenylmethoxy)-1-piperidinepropanamine were suspended in 20 ml of 1-butanol; 0.62 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 12 hours. After ice water and sodium hydrogen carbonate were added, the reaction mixture was extracted with ethyl acetate; the extract was washed with saturated saline and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol-triethylamine (90:10:1). The desired fraction was collected and concentrated; the crystal obtained was washed with ethyl acetate and dried to yield 0.648 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610694B1
Source datasetuspto-grants-2003_08
ORD IDord-4d3147e3bb5844ada7c54f1b19c9dd47
Source noteuspto-grants-2003_08