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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675108Generated: October 26, 2026

Fumaric Acid → 6-[4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine fumarate

https://huagongshe.com/reaction/1675108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
Reactant6-[4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazineHCID 44125972—
SolventAcetoneHCID 180—
Product6-[4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine fumarateHCID 67340922—

Reaction Steps

3 ml of acetone was added to 50 mg of 6-[4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine and heated to form a solution. 12.3 mg of fumaric acid was dissolved in 3 ml of acetone. The compound solution was added to the counter-ion solution and the resultant mixture shaken with heat. The solution was dried under air and once the volume had dramatically reduced, solid 6-[4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperazin-1-yl]-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine fumarate precipitated out.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-08df8d9a70c64afb83fbf25df15f733b
Source noteuspto-grants-2011_08