发明名称 Pyridine and pyrimidine derivatives
摘要 Compounds of formula (1) are described in which R<SUP>a </SUP>and R<SUP>b </SUP>is each independently a hydrogen atom or a group R<SUP>c</SUP>, or R<SUP>a </SUP>and R<SUP>b </SUP>together form an oxo (-O) or thio (-S) group; X is a N atom or an optionally substituted CH group: Y is a -O- or -S- atom or -SO- or -SO<SUB>2</SUB>- group or an optionally substituted -CH<SUB>2</SUB>- or -NH- group with the proviso that when R<SUP>a </SUP>and R<SUP>b </SUP>together form an oxo (-O) or thio (-S) group Y is an optionally substituted -CH<SUB>2</SUB>- or -NH-group; L<SUP>1 </SUP>is a covalent bond or a linker atom or group; p is zero or the integer 1; Alk<SUP>1 </SUP>is an optionally substituted C<SUB>1-10</SUB>aliphatic or C<SUB>1-10</SUB>heteroaliphatic chain; n is zero the integer 1, 2 or 3 with the proviso that when n is zero Y is an optionally substituted -CH<SUB>2</SUB>- group; Ar is an optionally substituted C<SUB>6-12</SUB>aromatic or C<SUB>1-9</SUB>heteroaromatic group; m is zero or the integer 1, 2 or 3; q is zero or the integer 1 or 2; R<SUP>1</SUP>, R<SUP>c </SUP>and R<SUP>d </SUP>are hydrogen atoms or the substituents described in the patent specification; and the salts, solvates, hydrates and N-oxides thereof. The compounds are potent and selective inhibitors of p38 kinase and are useful in the treatment of immune or inflammatory disorders.
申请公布号 US7323464(B2) 申请公布日期 2008.01.29
申请号 US20040495885 申请日期 2004.08.03
申请人 CELLTECH R&D LIMITED 发明人 DAVIS JEREMY MARTIN;LANGHAM BARRY JOHN;NAIK MANISHA;BROOKINGS DANIEL CHRISTOPHER;CUBBON RACHEL JANE;FRANKLIN RICHARD JEREMY
分类号 C07D403/04;A61K31/506;A61P29/00;C07D401/04;C07D403/14;C07D405/14;C07D409/14;C07D413/04;C07D413/14 主分类号 C07D403/04
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