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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674971Generated: October 30, 2026

Trifluoroacetic acid → 4-[[4-[3-(Trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]aniline

https://huagongshe.com/reaction/1674971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67339893HCID 67339893—
SolventDichloromethaneHCID 6344—
Product4-[[4-[3-(Trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperazin-1-yl]methyl]anilineHCID 5914975056.5%

Reaction Steps

A mixture of trifluoroacetic acid (0.5 mL, 0.15 mmol) and tert-butyl 4-((4-(3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazin-1-yl)methyl)phenylcarbamate (0.072 g, 0.15 mmol) in dichloromethane (2 mL) was stirred at ambient temperature for 2 hours and then evaporated to give an involatile residue. The residue was purified by hplc using a Phenomenex Luna C18 100A column (10μ silica, 21 mm diameter, 150 mm length) eluted with decreasingly polar mixtures of water (containing 0.1% TFA) and acetonitrile as eluents to give a partially purified product that was further purified by ion exchange chromatography using an SCX column eluted 7M aquous ammonia in methanol to give 4-((4-(3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazin-1-yl)methyl)aniline (0.032 g, 56.2%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-51798283efc547709a865393d41b31d7
Source noteuspto-grants-2011_08