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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169026Generated: October 26, 2026

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

https://huagongshe.com/reaction/1169026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloro-(1,2,4)triazolo(1,5-b)pyridazineHCID 11240611—
Reactant1-Piperidinebutanamine, 4-(diphenylmethoxy)-HCID 11739259—
Solvent1-ButanolHCID 263—
Product6-[4-[4-(Diphenylmethoxy)piperidino]butylamino][1,2,4]triazolo[1,5-b]pyridazineHCID 110049769.1%

Reaction Steps

4-(Diphenylmethoxy)-1-piperidinebutanamine (1.83 g) and 6-chloro[1,2,4]triazolo[1,5-b]pyridazine (557 mg) were dissolved in 1-butanol (30 ml), followed by addition of N-ethyldiisopropylamine (931 mg). The mixture was refluxed under heating for 14 hours. After being cooled, the mixture was concentrated under reduced pressure, followed by addition of ice-water 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 a silica gel column chromatography and eluted with a mixture of ethyl acetate, methanol and triethylamine (45:5:1). Fractions containing the objective compound were collected and concentrated. The resulting crystals were collected, washed with ethyl ether and dried to yield the title compound (149 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627630B1
Source datasetuspto-grants-2003_09
ORD IDord-a821833f505a4bc7b26d508fd2daf261
Source noteuspto-grants-2003_09