发明名称 PROCEDIMIENTO PARA LA OBTENCION DE NUEVOS DERIVADOS DEL ACIDO BENZOICO
摘要 <p>The benzoic acid derivatives according to the invention are specifically acting, adequately stable 5-lipoxygenase inhibitors and can be employed in particular in pharmaceutical preparations for the therapy of pathological conditions in which leukotrienes are involved as mediators. They correspond to the formula <IMAGE> in which A and E represent -C IDENTICAL C- and B and D represent -CH2-CH2- or A, B and D in each case represent -C IDENTICAL C- or cis-CH=CH- and E represents trans-CH=CH-, R1 is hydrogen, methyl or ethyl, R2 represents hydrogen, an alkyl or phenyl radical optionally substituted as defined or a cycloalkyl radical, R3 represents hydrogen, acetyl or propionyl and R4 represents a carboxyl group or a functional derivative thereof, such as a salt, an ester, an amide or a hydroxamic acid, or represents a nitrile group. The compounds of the formula I are in particular prepared according to the invention by synthesis of the aliphatic chain starting from suitable acetylene compounds. The radical R4 can then be converted into other desired carboxyl group derivatives. A, B, D and E can be varied within the context of the definition by partial or complete hydrogenation.</p>
申请公布号 ES553731(D0) 申请公布日期 1987.02.16
申请号 ES19310005537 申请日期 1986.04.04
申请人 GRUNENTHAL GMBH 发明人
分类号 C07C67/343;A61K31/165;A61K31/19;A61K31/195;A61K31/215;A61K31/22;A61K31/23;A61K31/235;A61K31/495;A61K31/535;A61P7/02;A61P9/00;A61P9/08;A61P9/10;A61P9/12;A61P11/08;A61P29/00;A61P37/08;A61P43/00;C07C33/04;C07C51/00;C07C51/347;C07C65/19;C07C67/00;C07C69/76;C07C69/767;C07C69/78;C07C213/00;C07C219/14;C07C231/00;C07C233/12;C07C235/42;C07C253/00;C07C255/53;C07C255/54;C07C259/06;C07D295/00;C07D295/18;C07D295/192;(IPC1-7):C07C69/78 主分类号 C07C67/343
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