362509-18-0Relevant articles and documents
Synthesis and biological evaluation of di-aryl urea derivatives as c-Kit inhibitors
Ravez, Séverine,Arsenlis, Stéphane,Barczyk, Amélie,Dupont, Anthony,Frédérick, Rapha?l,Hesse, Stéphanie,Kirsch, Gilbert,Depreux, Patrick,Goossens, Laurence
, p. 7340 - 7347 (2015)
Inhibition of receptor tyrosine kinases (RTKs) continued to be a successful approach for the treatment of many types of human cancers and many potent small molecules kinase inhibitors have been discovered the last decade. In the present study, we describe
Microwave-based synthesis of novel thienopyrimidine bioisosteres of gefitinib
Phoujdar, Manisha S.,Kathiravan, Muthu K.,Bariwal, Jitender B.,Shah, Anamik K.,Jain, Kishor S.
, p. 1269 - 1273 (2008/09/18)
A series of novel 2-unsubstituted 4-(substituted)anilinothieno[2,3-d]pyrimidines is synthesized through the chlorination of the corresponding 2-unsubstituted-thieno[2,3-d]-pyrimidin-4-ones, followed by the nucleophilic displacement of the 4-Cl group of 9, with a variety of anilines. All four steps of this synthesis involve microwave irradiation (MWI) and the entire synthesis requires only 2 h.