发明名称 Pyrimidinone compounds and methods for treating influenza
摘要 In one aspect, the invention relates to novel, broad-spectrum anti-viral, pyrimidinone compounds, methods of use, compositions and kits useful in treating and/or preventing influenza. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
申请公布号 US9328075(B2) 申请公布日期 2016.05.03
申请号 US201214115560 申请日期 2012.05.05
申请人 St. Jude Children's Research Hospital 发明人 Webb Thomas R.;Boyd Vincent A.
分类号 C07D239/54;C07D401/04;C07D401/12;C07D403/04;C07D487/04;A61K31/13;A61K31/59;A61K38/21;A61K45/06;A61K31/4045;A61K31/5377;A61K31/7012;A61K31/551;A61K31/505;A61K31/506;A61K31/519;A61K31/196;A61K31/215;A61K31/351 主分类号 C07D239/54
代理机构 Ballard Spahr LLP 代理人 Ballard Spahr LLP
主权项 1. A compound of the formula: wherein R1 is an optionally substituted heteroaryl; wherein R3 is optionally substituted and selected from cycloalkyl, heterocycloalkyl, aryl, heteroaryl, —CONR4R5, and —COR6; wherein R4 and R5 are each optionally substituted and independently selected from hydrogen, alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl; wherein at least one of R4 or R5 is not hydrogen, and provided that when R1 is a heteroaryl group having 6 or more ring members, then neither R3 nor R4 is hydrogen; or wherein —NR4R5 together form an optionally substituted ring selected from piperidinyl, morpholinyl, and piperazinyl; and wherein R6 is optionally substituted and selected from alkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, phenyl, pyridazinyl, pyrimidyl, pyrazyl, triazinyl, pyrrolyl, pyrazolyl, imidazolyl, (1,2,3,)- and (1,2,4)-triazolyl, pyrazinyl, pyrimidinyl, tetrazolyl, thienyl, isoxazolyl, thiazolyl, and oxazolyl, or a pharmaceutically acceptable salt thereof.
地址 Memphis TN US