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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675055Generated: November 3, 2026

Lithium hydroxide, monohydrate → 4-[[1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]oxy]benzoic acid

https://huagongshe.com/reaction/1675055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 4-[[1-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]oxy]benzoateHCID 67340092—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-[[1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]oxy]benzoic acidHCID 6734050397.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

Lithium hydroxide monohydrate (0.488 g, 20.40 mmol) was added to ethyl 4-[[1-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]oxy]benzoate (2.22 g, 5.10 mmol) in MeOH (80 mL) and water (40.0 mL). The resulting suspension was stirred at 50° C. for 2 days. The reaction was cooled to room temperature, the methanol was evaporated and the aqueous residues treated with citric acid until precipitation ceased. The precipitate was collected by filtration, washed with water and dried to afford 4-[[1-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-yl]oxy]benzoic acid (2.020 g, 97%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-e65e39f7d2a240499f8a1ce909a675ef
Source noteuspto-grants-2011_08