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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169023Generated: October 25, 2026

4-Benzhydryl-1-piperazinepropanol → 6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochloride

https://huagongshe.com/reaction/1169023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzhydryl-1-piperazinepropanolHCID 15524146—
Reactant6-Chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazineHCID 22989227—
ReactantSodium t-butoxideHCID 23676156—
SolventTetrahydrofuranHCID 8028—
Product6-[3-[4-(Diphenylmethyl)piperazino]propoxy]-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine dihydrochlorideHCID 22989368142.7%

Reaction Steps

4-(Diphenylmethyl)-1-piperazinepropanol (466 mg) was dissolved in dried tetrahydrofuran (10 ml), followed by addition of sodium t-butoxide (173 mg). The mixture was refluxed under heating for 30 minutes. After the mixture was cooled, 6-chloro-7-isopropyl[1,2,4]triazolo[1,5-b]pyridazine (295 mg) was added thereto. The resulting mixture was refluxed for 3 hours under heating. After cooling, ice-water was added to the mixture, followed by 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 and methanol (10:1). Fractions containing the objective compound were collected and dissolved in ethanol (10 ml), followed by addition of 1N-HCl (3 ml). The mixture was concentrated under reduced pressure. The resulting crystals were recrystallized from ethyl acetate to yield the title compound (582 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627630B1
Source datasetuspto-grants-2003_09
ORD IDord-78d399a7f2ac435590a5d11c96adc963
Source noteuspto-grants-2003_09