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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486459Generated: October 28, 2026

3,6-Dichloropyridazine → HCID 19095533, compound

https://huagongshe.com/reaction/486459

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 numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-bf36a5459c3043c7811befb0211ebefb
Source noteuspto-grants-1994_03