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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705416Generated: October 25, 2026

Triethylamine → Enzalutamide carboxylic acid

https://huagongshe.com/reaction/705416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Isothiocyanato-2-(trifluoromethyl)benzonitrileHCID 11615540—
Reactant4-(2-Carboxypropan-2-ylamino)-2-fluorobenzoic acidHCID 67395503—
SolventEthanolHCID 702—
ProductEnzalutamide carboxylic acidHCID 468985222.2%

Reaction Steps

4-(1-Carboxy-1-methyl-ethylamino)-2-fluoro-benzoic acid (241 mg, 1 mmol), 4-isothiocyanato-2-trifluoromethylbenzonitrile (342 mg, 1.5 mmol) and triethylamine (343 mg, 3.4 mmol) were mixed in EtOH (5 mL) and the solution was stirred for 10 days at room temperature. The reaction mixture was concentrated under reduced pressure, the residue was acidified with 1M aqueous HCl, and the product was extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product obtained was purified by column chromatography eluting with ethyl acetate to obtain 4-[3-(4-cyano-3-trifluoromethyl-phenyl)-5,5-dimethyl-4-oxo-2-thioxo-imidazolidin-1-yl]-2-fluoro-benzoic acid (10 mg) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174943B2
Source datasetuspto-grants-2015_11
ORD IDord-53a62065c1ab4682a5a859b9df82a20c
Source noteuspto-grants-2015_11