发明名称 1-substituted imidazoles, and salts thereof, a method for their preparation and pharmaceutical formulations thereof.
摘要 <p>Imidazoles of formula (I) &lt;Chemistry id="chema01" num="0001"&gt;&lt;Image id="ia01" he="16" wi="48" file="IMGA0001.TIF" imgContent="chem" imgFormat="TIFF" inline="no" /&gt;&lt;/Chemistry&gt;wherein A is a chemical bond or a straight or branched, saturated or unsaturated, aliphatic residue having from 1 to 6 carbon atoms, optionally substituted and/or optionally including 1, 2 or3 heteroatoms selected from oxygen, sulphur and nitrogen providing (in the case of 2 or 3 heteroatoms) that any such heteroatom is not located adjacent to a further such heteroatom or heteroatoms, the total number of said carbon atoms and heteroatoms not exceeding 6.</p><p>R is a fused, saturated or unsaturated, non-aromatic carbocyclic, bi- or tri-cyclic ring system providing that when R is a 9- decahydronaphthyl group, A does not represent a carbonyl group, a saturated or unsaturated, carbocyclic spirocyclic ring system, optionally containing one or more ring heteroatoms selected from oxygen, sulphur and nitrogen; or a saturated or unsaturated. carbocyclic bridged-polycyclic ring system, optionally containing one or more ring heteroatoms selected from oxygen, sulphur and nitrogen and having one or more bridges providing that when R is an adamantanyl group, A does not represent an ethylene radical (-(CH&lt;Sub&gt;2&lt;/Sub&gt;)&lt;Sub&gt;2&lt;/Sub&gt;-) substituted at the carbon atom a to the adamantanyl group by a hydroxy, oxo, ether or thioether grouping; or AR together represent a straight or branched, saturated or unsaturated, aliphatic residue having 3 to 6 carbon atoms, optionally substituted and/or optionally including 1, 2 or 3 heteroatoms selected from oxygen, sulphur and nitrogen providing (in the case of 2 or 3 heteroatoms) that any such heteroatom is not located adjacent to a further such heteroatom or heteroatoms, the total number of said carbon and heteroatoms not exceeding 6; which aliphatic residue is substituted by at least two groups, which may be the same or different, selected from the groups specified for R above and acid addition salts and pharmaceutically acceptable bioprecursors thereof.</p><p>Methods of preparing the imidazoles are disclosed</p><p>The imidazoles and their acid addition salts an bioprecur. sors are useful in the treatment of prophylaxis of thrombo- embolic conditions.</p>
申请公布号 EP0015002(A1) 申请公布日期 1980.09.03
申请号 EP19800100869 申请日期 1980.02.21
申请人 THE WELLCOME FOUNDATION LIMITED 发明人 THOROGOOD, PETER BRIAN
分类号 C07D233/64;A61K31/415;A61K31/47;A61K31/52;A61K31/585;A61P7/02;C07C29/14;C07C29/40;C07D233/56;C07D233/58;C07D233/60;C07D317/72;C07D405/06;C07D451/02;C07D453/02;C07D521/00;(IPC1-7):07D233/58;07D233/60;61K31/415;07D471/08;07D405/06 主分类号 C07D233/64
代理机构 代理人
主权项
地址