发明名称 TERAPEUTISK AKTIVE PYRIMIDINDERIVATER OG FREMGANGSMAATE FOR DERES FREMSTILLING
摘要 <p>Novel pyrimidine derivatives and pharmacologically acceptable salts thereof are disclosed which exhibit excellent antitumor activity, and are represented by the following general formula: (I) wherein R1 represents a hydroxyl or amino group; R2 represents a phenylene, pyridinediyl, thiendiyl, furandiyl or thiazoldiyl group, -CO2R5 and -CO2R6 may be the same or different from each other and each represents a carboxyl group or a carboxylic acid ester, the part X-Y-Z represents , or , A represents an oxygen atom, a group represented by the formula: (wherein R3 and R4 may be the same or different from each other and each represents a hydrogen or halogen atom or a hydro-carbon group which may be substituted, or alternatively R3 and R4 may be united to form an alkylidene group which may be substituted) or a group represented by the formula: (wherein R70 represents a hydrogen atom or a hydrocarbon group), and n is an integer of 1 to 3, provided that the compound in which R1 represents oxygen, and hydrogen is attached to nitrogen at 3-position is included in the above shown definition. Processes for preparation of the derivatives (I) and their salts are also disclosed, as well as antitumor drugs containing the same.</p>
申请公布号 NO923249(D0) 申请公布日期 1992.08.19
申请号 NO19920003249 申请日期 1992.08.19
申请人 EISAI CO LTD 发明人 NOMURA HIROAKI;HANEDA TORU;KOTAKE YOSHIHIKO;UEDA NORIHIRO;KITOH KYOSUKE
分类号 A61K31/505;A61K31/495;A61K31/517;A61K31/519;A61P35/00;C07D;C07D239/70;C07D239/86;C07D239/90;C07D401/06;C07D401/08;C07D401/12;C07D405/06;C07D405/08;C07D405/12;C07D409/06;C07D409/08;C07D409/12;C07D417/06;C07D417/08;C07D417/12;C07D487/04;(IPC1-7):C07D/ 主分类号 A61K31/505
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