Original document(24 pages)  中文版
    Compounds of formula (I) in free or salt form, where Ar is phenyl substituted by one or more substituents selected from halogen, cyano and C1- C8-haloalkyl, or naphthyl, R<1> is hydrogen, phenyl optionally substituted by one or more substituents selected from halogen, cyano, hydroxy, C1-C8-alkyl, C1-C8-haloalkyl, C1-C8-alkoxy, C1-C8-alkoxy-Cl-C8 alkyl, carboxy, C1-C8-alkoxycarbonyl and acyloxy, or R<1> is a 5- or 6- membered monovalent heterocyclic group, R<2> is hydrogen, Cl-C8-alkyl, acyl or -CON(R<3>)R<4>, R<3> and R<4> are each independently hydrogen or C1-Cs-alkyl, or together with the nitrogen atom to which they are attached denote a 5- or 6- membered heterocyclic group, and Y is a pyrimidinyl or pyridazinyl group, optionally substituted by at least one C1-Cs-alkyl, C1-C8-alkoxy, C1-C8-alkylthio, C1-C8-alkyl amino, di(Cl-C8-alkyl) amino or acylamino group. The compounds are useful as pharmaceuticals.
Application Number
申请号
200580002688 Application Date
申请日
2005.01.20
Title 名称 Thiazole derivatives as A2B antagonists
Publication Number
公开号
1910178 Publication Date
公开日
2007.02.07
Approval Pub. Date Granted Pub. Date
International Classification 分类号 C07D417/04;C07D417/14;A61K31/501;A61K31/506;A61P11/00
Applicant(s) Name
申请人
Novartis AG
Address 地址
Inventor(s) Name 发明人 Press Neil John;Taylor Roger John
Attorney & Agent 代理人 huang gesheng lin bainan
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