发明名称 UN PROCEDIMIENTO PARA PREPARAR UN COMPUESTO HETEROCICLICO NITROGENADO
摘要 <p>Compounds of the formula (I) : <CHEM> or pharmaceutically acceptable salts thereof, wherein : <??>R<1> and R<2> are independently C1-4alkyl; or R<1> and R<2> together with the nitrogen atom to which they are joined represent a pyrrolidino, piperidino or hexahydroazepino ring; Y is straight-chain or branched-chain C1-4alkyl; n is 2 to 5; m is 0 or 1; when m is 1, Z is inter alia an optionally substituted pyridine, pyrimidine, oxazole, thiazole, imidazole, benzoxazole benzthiazole or N-alkylbenzimidazole ring; when m is 0, Z is an optionally substituted imidazole, pyrazole or benzimidazole ring. <??>The compounds are histamine H2-receptors antagonists and relatively lipophilic and can penetrate the blood-brain barrier and are useful in treating diseases mediated via histamine H2- receptors. Processes for their preparation, pharmaceutical compositions and methods of use are described. </p>
申请公布号 ES548448(D0) 申请公布日期 1987.01.01
申请号 ES19480005484 申请日期 1985.10.31
申请人 SMITH KLINE & FRENCH LABORATORIES LIMITED 发明人
分类号 A61K31/415;A61K31/4184;A61K31/425;A61K31/426;A61K31/428;A61K31/44;A61K31/4402;A61K31/4406;A61K31/4409;A61K31/4412;A61K31/4418;A61K31/445;A61K31/454;A61K31/47;A61K31/472;A61P1/04;A61P43/00;C07D;C07D213/74;C07D213/89;C07D215/38;C07D215/42;C07D217/22;C07D231/12;C07D231/20;C07D233/54;C07D233/64;C07D233/88;C07D235/12;C07D235/30;C07D239/42;C07D239/86;C07D239/94;C07D263/58;C07D277/20;C07D277/42;C07D277/82;C07D295/08;(IPC1-7):C07D277/82;A61K31/42 主分类号 A61K31/415
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