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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351645Generated: November 1, 2026

1-(3-(Trifluoromethyl)phenyl)piperazine → HCID 14390218, compound

https://huagongshe.com/reaction/2351645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-chlorophenyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390457—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14390218HCID 1439021847.2%

Reaction Steps

A suspension of 2-(4-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (4.0 g, 0.014 mole), 1,1'-carbonyldiimidazole (2.3 g, 0.014 mole), and anhydrous tetrahydrofuran (100 ml) was stirred at room temperature with a stream of nitrogen bubbling through the mixture for 21/2 hrs. A solution of N-(α, α, α-trifluoro-m-tolyl)-piperazine (3.2 g, 0.014 mole) in dry tetrahydrofuran (10 ml) was added and the reaction mixture was stirred at room temperature for 41/2 hrs. The tetrahydrofuran was evaporated and the residue dissolved was extracted with 5% potassium hydroxide solution (2×30 ml), water (30 ml), brine (25 ml), dried over sodium sulfate, and concentrated in vacuo. The residue (6.6 g) was twice recrystallized from isopropyl alcohol-isopropyl ether to give 3.3 g (47%) of white needles, mp 185°-186.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873251
Source datasetuspto-grants-1989_10
ORD IDord-0336ed447bcd47d28e8e560a2e483d9f
Source noteuspto-grants-1989_10