发明名称 PROCEDIMIENTO DE PREPARAR NUEVAS DIAZEPINONAS CONDENSADAS
摘要 <p>Disclosed are novel condensed diazepinones of formula I <IMAGE> wherein B is a fused ring selected from <IMAGE> X is -CH- or, when B is ortho-phenylene, X can also be nitrogen; A1 is C1-C2 alkylene; A2 is C1-C2 when it is in the 2-position relative to the saturated heterocyclic ring nitrogen or a single bond or methylene when it is in the 3- or 4-position; R1 is C1-C3 alkyl; R2 is C1-C7 alkyl, optionally hydroxy-substituted on at least one of its second to seventh carbon, or C3-C7 cycloalkyl, optionally hydroxy substituted, or C3-C7 cycloalkylmethyl; or R1 and R2 can, together with the nitrogen therebetween, be a 4- to 7-membered saturated monocyclic, heterocyclic ring which can optionally include an oxygen or N-CH3; R3 is hydrogen, chlorine, or methyl; R4 is hydrogen or C1-C4 alkyl, R5 is hydrogen, chlorine or C1-C4 alkyl; and Z is a single bond, oxygen, methylene or 1,2-ethylene; and NR1 R2-N oxides and nontoxic, pharmaceutically acceptable addition salts thereof. Also disclosed are pyrrolobenzodiazepinone intermediates, pharmaceutical compositions containing the condensed diazepinones and methods of using them to treat cardiovascular disorders, particularly bradycardia and bradyarrhythmia.</p>
申请公布号 ES551277(D0) 申请公布日期 1987.01.16
申请号 ES19770005512 申请日期 1986.01.27
申请人 DR. KARL THOMAE GESELLSCHAFT MIT BESCHRANKTER HAF 发明人
分类号 A61K31/00;A61K31/55;A61P9/06;A61P25/02;C07D207/09;C07D207/16;C07D207/34;C07D211/26;C07D213/38;C07D223/04;C07D223/08;C07D223/12;C07D243/00;C07D243/14;C07D243/38;C07D401/06;C07D401/12;C07D401/14;C07D403/06;C07D403/14;C07D413/06;C07D413/14;C07D471/04;C07D487/04;C07D495/04;C07D495/14;(IPC1-7):C07D401/06 主分类号 A61K31/00
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