发明名称 UN PROCEDIMIENTO DE OBTENCION DE IMIDAZOQUINOLINAS CONTE- NIENDO OTROS GRUPOS HETEROCICLICOS
摘要 <p>The invention provides novel imidazoquinolines, processes for their preparation and pharmaceutical compositions containing them. The compounds have Formula I <CHEM> wherein A is a C1-C4 straight or branched alkylene chain which may be saturated or unsaturated, B is a C2-C4 straight or branched alkylene chain which may be saturated or unsaturated, R<1> and R<2> are the same or different and are hydrogen, alkyl, alkoxy, alkoxyalkyl, hydroxyalkyl, hydroxy, halogen, nitro, carboxy, carboxylic ester, carbamoyl, carbamoyloxy, cyano, acyl, acylamino or trifluoromethyl, Het is a heterocyclic group chosen from imidazolyl, imidazolinyl, benzimidazolyl, thiazolyl, thiazolinyl, quinolyl, piperidyl, pyridyl, benzothiazolyl and pyrimidyl, any of which heterocyclic groups may be substituted, and x is 0 or 1, and pharmaceutically acceptable salts thereof. The compounds are anti-ulcer/anti-secretory agents.</p>
申请公布号 ES550592(D0) 申请公布日期 1987.04.01
申请号 ES19920005505 申请日期 1985.12.31
申请人 JOHN WYETH & BROTHER LIMITED 发明人
分类号 C07D471/06;C07D487/06;(IPC1-7):C07D471/06;A61K31/47 主分类号 C07D471/06
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