发明名称 Rilyazine derivatives and compositions for the treatment of cancer
摘要 The present application discloses Rilyazine analogs, methods for their preparation, and the treatment of cancer by the administration of an effective amount of the Rilyazine analogs to a patient in need thereof.
申请公布号 US9394299(B2) 申请公布日期 2016.07.19
申请号 US201414473472 申请日期 2014.08.29
申请人 Warner Babcock Institute for Green Chemistry, LLC 发明人 Warner John C.;Gladding Jeffery A.;Gero Thomas W.;Cheruku Srinivasa R.
分类号 C07D471/04 主分类号 C07D471/04
代理机构 Cermak Nakajima & McGowan LLP 代理人 Cermak Nakajima & McGowan LLP ;McGowan Malcolm K.
主权项 1. A compound selected from the group consisting of: wherein: each R1 is independently selected from the group consisting of hydrogen, halo, nitro, trifluoromethyl, trifluoromethoxy, methoxy, carboxy, —NH2, —OH, —SH, —NHCH3, —N(CH3)2, —SCH3, —CN, (C1-C6)alkyl, substituted (C1-C6)alkyl, aryl and heteroaryl; each R2 is independently selected from the group consisting of hydrogen, (C1-C12)alkyl, (C1-C12)alkoxy, —C(O)(C1-C12)alkyl, (C3-C10)cycloalkyl, aryl, aryloxy, heteroaryl and heteroaryloxy, wherein each of (C1-C12)alkyl, (C1-C12)alkoxy, —C(O)(C1-C12)alkyl, (C3-C10)cycloalkyl, aryl, aryloxy, heteroaryl and heteroaryloxy is unsubstituted or substituted with 1 or 2 substituents selected from the group consisting of halo, nitro, trifluoromethyl, trifluoromethoxy, methoxy, carboxy, —NH2, —OH, —SH, —NHCH3, —N(CH3)2, -SCH3, —CN, (C1-C6)alkyl, substituted (C1-C6)alkyl, aryl and heteroaryl; and each R3 is independently selected from the group consisting of hydrogen, halo, nitro, trifluoromethyl, trifluoromethoxy, methoxy, carboxy, —NH2, —OH, —SH, —NHCH3, —N(CH3)2, —SCH3, —CN, (C1-C6)alkyl, substituted (C1-C6)alkyl, aryl and heteroaryl; as a single stereoisomer, a mixture of stereoisomers, and a pharmaceutically acceptable salt thereof.
地址 Wilmington MA US