| CPC C07D 405/12 (2013.01) [A61K 31/343 (2013.01); A61K 31/381 (2013.01); A61K 31/382 (2013.01); A61K 31/4035 (2013.01); A61K 31/416 (2013.01); A61K 31/427 (2013.01); A61K 31/437 (2013.01); A61K 31/443 (2013.01); A61K 31/4525 (2013.01); A61K 31/506 (2013.01); A61K 31/517 (2013.01); A61K 31/519 (2013.01); A61K 31/5377 (2013.01); A61K 31/5386 (2013.01); A61K 31/541 (2013.01); C07D 307/81 (2013.01); C07D 307/83 (2013.01); C07D 403/12 (2013.01); C07D 405/14 (2013.01); C07D 409/12 (2013.01); C07D 409/14 (2013.01); C07D 413/14 (2013.01); C07D 417/12 (2013.01); C07D 471/04 (2013.01); C07D 487/04 (2013.01); C07D 491/107 (2013.01); C07D 498/10 (2013.01)] | 16 Claims |
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1. A method of treating an endometrial cancer in a human subject, the endometrial cancer having one or more mutations in PI3Kα, the method comprising administering to the subject a therapeutically effective amount of a compound which is 1-(2-aminopyrimidin-5-yl)-3-(1-(5,7-difluoro-3-methylbenzofuran-2-yl)-2,2,2-trifluoroethyl) urea, or a pharmaceutically acceptable salt thereof, having the structure:
![]() or a pharmaceutically acceptable salt thereof.
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