To provide a synthesis method that can be easily used to prepare tri- and tetra-substituted pyrimidine derivatives in a large amount, moreover to provide a method that uses a starting material that uses the minimum process and can be easily acquired, and a simple reaction medium.
The present invention provides a facile process for the preparation of tri- and tetra-substituted pyrimidines. The process is useful for preparing inhibitors of protein kinases, especially Aurora kinase. These inhibitors are useful for treating or lessening the severity of Aurora-mediated diseases or conditions. The present invention provides a method that treats a cancer of a patient, and the method includes a process in which a compound of a formula V or a composition thereof is administrated to the patient.
MAZZEI FRANCESCA
KAY DAVID
MILLER ANDREW
JP4210520B2 | 2009-01-21 | |||
JP4237701B2 | 2009-03-11 |
Natsuki Morishita
Next Patent: SUBSTITUTED IMIDAZO[1,2B]PYRIDAZINE COMPOUND AS TRK KINASE INHIBITOR