Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329404Generated: October 26, 2026

Sodium Iodide → 4-(4-(2-(4-(3-Trifluoromethylphenyl)piperazinyl)ethyl)phenyl)-2-methylthiazole

https://huagongshe.com/reaction/329404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantTFMPP hydrochlorideHCID 3084246—
Reactant4-(4-(2-Chloroethyl)phenyl)-2-methylthiazole hydrobromideHCID 14726991—
SolventMethyl Isobutyl KetoneHCID 7909—
Product4-(4-(2-(4-(3-Trifluoromethylphenyl)piperazinyl)ethyl)phenyl)-2-methylthiazoleHCID 14727014—

Reaction Steps

To a 125 ml round-bottomed flask equipped with condenser and N2 inlet were added 2.39 g (7.5 mmol) of 4-(4-(2-chloroethyl)phenyl)-2-methylthiazole hydrobromide, 2.0 g (7.5 mmol) of N-(3-trifluoromethylphenyl)piperazine hydrochloride, 2.62 ml (15.0 mmol) of diisopropylethylamine, 1.59 g (15.0 mmol) of sodium carbonate, 5 mg of sodium iodide, and 50 ml of methylisobutylketone. The reaction was heated at reflux for 4.5 days, filtered hot to remove inorganic material, cooled, and the precipitate filtered and washed with ether and ethyl acetate. The solid was taken up in methylene chloride, hydrochloride gas bubbled through to precipitate the salt, and the resulting solid filtered, washed with methylene chloride, and dried to give a solid, m.p. 170°-175° C., 1.93 g (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891375
Source datasetuspto-grants-1990_01
ORD IDord-657c9b01e2664e808756328b3d3ef8e0
Source noteuspto-grants-1990_01