Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359431Generated: November 1, 2026

3,6-Dichloropyridazine → HCID 19095533, compound

https://huagongshe.com/reaction/359431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-DichloropyridazineHCID 67331—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 19095533HCID 1909553345.3%

Reaction Steps

A mixture of 3.3 parts of 3,6-dichloropyridazine, 3.3 parts of 1-(2-pyridinyl)piperazine, 1.5 parts of sodium hydrogencarbonate and 120 parts of ethanol was stirred and refluxed over weekend. The reaction mixture was evaporated. Water was added to the residue and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanol and tetrahydrofuran, yielding 2.5 parts (45.3%) of 3-chloro-6-[4-(2-pyridinyl)-1-piperazinyl]pyridazine; mp. 194.7° C. (compound 213).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001125
Source datasetuspto-grants-1991_03
ORD IDord-e960b7abfa4d4af3b75d6a7bcde3f857
Source noteuspto-grants-1991_03