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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231771Generated: October 30, 2026

3-(Piperazin-1-yl)propane-1,2-diol → HCID 20032015, compound

https://huagongshe.com/reaction/231771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Piperazin-1-yl)propane-1,2-diolHCID 111002—
Reactant3-Chloropyridazine-4-carbonitrileHCID 12370972—
SolventHydrochloric AcidHCID 313—
SolventIsopropanolHCID 3776—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20032015HCID 20032015—

Reaction Steps

Grams 6.9 of 1-(2,3-dihydroxypropyl)piperazine and 3.0 g of 4-cyano-3-chloropyridazine in 60 ml dioxane were refluxed for 2 hours. The reaction mixture was settled, the supernatant liquor evaporated to dryness and the residue, which formed, was dissolved in 10 ml concentrated hydrochloric acid and diluted with 10 volumes of isopropanol. A precipitate was obtained formed by a gummy oil, which solidified afterwards giving 5.9 g of 3-[4-(4-cyanopyridazin-3-yl)piperazin-1yl]propane-1,2-diol dihydrochloride which melted at 128°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849422
Source datasetuspto-grants-1989_07
ORD IDord-f2986ccf2e044ec0b57fdf96135df790
Source noteuspto-grants-1989_07