HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705416Generated: October 25, 2026
Triethylamine → Enzalutamide carboxylic acid
https://huagongshe.com/reaction/705416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Isothiocyanato-2-(trifluoromethyl)benzonitrile | HCID 11615540 | — |
| Reactant | 4-(2-Carboxypropan-2-ylamino)-2-fluorobenzoic acid | HCID 67395503 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Enzalutamide carboxylic acid | HCID 46898522 | 2.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174943B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-53a62065c1ab4682a5a859b9df82a20c |
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| Source note | uspto-grants-2015_11 |
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