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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397557Generated: October 25, 2026

Ethyl Acetate → 6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/397557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
Reactant1-Piperidinebutanamine, 4-(diphenylmethoxy)-HCID 11739259—
Solvent1-ButanolHCID 263—
Product6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[4,3-b]pyridazineHCID 1552415139.4%

Reaction Steps

1.15 g of 4-(diphenylmethoxy)-1-piperidinebutanamine and 578 mg of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine were dissolved in 20 ml of 1-butanol; 1.17 ml of N-ethyldiisopropylamine was added, followed by refluxing under heating for 14 hours. After cooling, ethyl acetate was added; the reaction mixture was washed with aqueous sodium bicarbonate and 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 (50:5:1). The desired fraction was collected and concentrated under reduced pressure; the residue was crystallized from ethyl acetate and dried to yield 611 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610694B1
Source datasetuspto-grants-2003_08
ORD IDord-b5bf99c2ffe947f096ecd639dfe4e842
Source noteuspto-grants-2003_08