Diarylthiohydantoin compound as androgen receptor antagonist
US-2023035184-A1 · Feb 2, 2023 · US
US12358913B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12358913-B2 |
| Application number | US-202017427496-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2020 |
| Priority date | Feb 1, 2019 |
| Publication date | Jul 15, 2025 |
| Grant date | Jul 15, 2025 |
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The present application belongs to the field of medicine, and in particular relates to a crystal of a diarylthiohydantoin compound, a preparation method therefor, and use thereof in the preparation of medicaments for treating related diseases which are androgen-mediated.
Opening claim text (preview).
The invention claimed is: 1. A crystal of a compound of formula I, wherein, in an X-ray powder diffraction pattern using Cu Kα radiation, diffraction peaks exist at 2θ of 13.47°±0.2°, 15.32°±0.2°, 15.98°±0.2°, 18.68°±0.2°, 23.11°±0.2° and 26.41°±0.2°. 2. The crystal of the compound of formula I according to claim 1 , wherein the crystal having an absorption peak at 238.92° C. according to differential scanning calorimetry analysis thereof 3. A crystalline composition, comprising no less than 50 wt % of the crystal of the compound of formula I according to claim 1 . 4. A pharmaceutical composition, comprising a therapeutically effective amount of the crystal of the compound of formula I according to claim 1 . 5. The crystal of the compound of formula I according to claim 1 , wherein, in an X-ray powder diffraction pattern using Cu Kα radiation, diffraction peaks exist at 2θ of 13.01°±0.2°, 13.47°±0.2°, 14.00°±0.2°, 15.32°±0.2°, 15.98°±0.2°, 18.68°±0.2°, 22.78°±0.2°, 23.11°±0.2°, 24.49°±0.2° and 26.41°±0.2°. 6. The crystalline composition according to claim 3 , comprising no less than 80 wt % of the crystal of the compound of formula I according to claim 1 . 7. The crystalline composition according to claim 6 , comprising no less than 90 wt % of the crystal of the compound of formula I according to claim 1 . 8. The crystalline composition according to claim 7 , comprising no less than 95 wt % of the crystal of the compound of formula I according to claim 1 . 9. The pharmaceutical composition according to claim 4 , comprising a pharmaceutically acceptable excipient.
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