发明名称 AMINOTHIAZOLES AND THEIR USE AS ADENOSINE RECEPTOR ANTAGONISTS
摘要 Compounds of formula (I) in free or salt form, where A is a C<SUB>6</SUB>-C<SUB>15 </SUB>monovalent aromatic group. R<SUP>1 </SUP>is hydrogen, phenyl optionally substituted by one or more substituents selected from halogen, cyano, hydroxy, C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl, C<SUB>1</SUB>-C<SUB>8</SUB>-haloalkyl, C<SUB>1</SUB>-C<SUB>8</SUB>-alkoxy, C<SUB>1</SUB>-C<SUB>8</SUB>-alkoxy-C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl or acyloxy, or a 5- or 6-membered monovalent heterocyclic group, R<SUP>2 </SUP>is hydrogen, C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl, acyl or CON(R<SUP>3</SUP>)R<SUP>4</SUP>, provided that R<SUP>2 </SUP>is C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl, acyl or CON(R<SUP>3</SUP>)R<SUP>4 </SUP>when R<SUP>1 </SUP>is hydrogen, R<SUP>3 </SUP>and R<SUP>4 </SUP>are each independently hydrogen, or C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl, together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclic group, and Z<SUP>l</SUP>, Z<SUP>2</SUP>, Z<SUP>3 </SUP>and Z<SUP>4 </SUP>are each independently N or CR<SUP>5</SUP>, at least one of them being CR<SUP>5</SUP>, and R<SUP>5 </SUP>is hydrogen, C<SUB>1</SUB>-C<SUB>8</SUB>-alkyl or C<SUB>1</SUB>-C<SUB>8</SUB>-alkoxy. The compounds are useful as adenosine receptor antagonists, particularly in the treatment of inflammatory or obstrucive airways diseases
申请公布号 KR20040007412(A) 申请公布日期 2004.01.24
申请号 KR20037006156 申请日期 2003.05.02
申请人 发明人
分类号 C07D417/04;A61K31/427;A61K31/4439;A61K31/497;A61K45/00;A61P1/04;A61P1/12;A61P1/16;A61P3/10;A61P7/00;A61P7/06;A61P9/10;A61P11/00;A61P11/02;A61P11/06;A61P11/08;A61P13/12;A61P17/00;A61P17/06;A61P17/14;A61P17/16;A61P19/00;A61P21/04;A61P25/28;A61P27/02;A61P27/06;A61P27/14;A61P29/00;A61P35/00;A61P37/02;A61P37/08;A61P43/00;C07D417/14;C07D521/00 主分类号 C07D417/04
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