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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674777Generated: October 31, 2026

4-[(Piperazin-1-yl)methyl]benzonitrile → 4-((4-(7-Methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazin-1-yl)methyl)benzonitrile

https://huagongshe.com/reaction/1674777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(Piperazin-1-yl)methyl]benzonitrileHCID 2060892—
Reactant6-Chloro-7-methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 53629201—
Product4-((4-(7-Methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazin-1-yl)methyl)benzonitrileHCID 6734096375%

Reaction Steps

The method of Example 12 was repeated using a mixture of 6-chloro-7-methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine (0.078 g, 0.33 mmol) and 1-(4-cyanobenzyl)-piperazine (0.199 g, 0.99 mmol) to give 4-((4-(7-methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazin-1-yl)methyl)benzonitrile (0.099 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-d22a27defa1c424a961f82fb763a016c
Source noteuspto-grants-2011_08