首页> 外国专利> Esters of derivatives of 2-alpha-hydroxy-substituted 4-hydroxy-3-quinoline carboxylic acid, their preparation, their use as medicaments and compositions containing them.

Esters of derivatives of 2-alpha-hydroxy-substituted 4-hydroxy-3-quinoline carboxylic acid, their preparation, their use as medicaments and compositions containing them.

机译:2-α-羟基取代的4-羟基-3-喹啉羧酸的衍生物的酯,它们的制备,它们作为药物的用途和包含它们的组合物。

摘要

Novel optical isomers and racemates of 4-hydroxy-3-quinoline-carboxylates of the formula IMAGE I wherein X is in the 5-, 6-, 7- or 8-position and is selected from the group consisting of hydrogen, halogen, alkyl of 1 to 5 carbon atoms, alkoxy of 1 to 4 carbon atoms, -CF3, -SCF3 and -OCF3, R1 is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, R2 is selected from the group consisting of thiazolyl, 4,5-dihydrothiazolyl, pyridinyl, oxazolyl, isoxazolyl, imidazolyl, pyrimidyl and tetrazolyl all optionally substituted with alkyl of 1 to 4 carbon atoms and phenyl substituted with at least one member of the group consisting of -OH, alkyl and alkoxy of 1 to 4 carbon atoms, -CF3, -NO2 and halogen, R3 and R4 are individually selected from the group consisting of hydrogen, alkyl of 1 to 4 carbon atoms and aryl, R5 is selected from the group consisting of aryl of 6 to 14 carbon atoms, heteroaryl of 3 to 14 carbon atoms, alkyl of 1 to 14 carbon atoms, alkyl substituted with -NH2, -NHAlk or IMAGE alkenyl of 2 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms substituted with aryl of 6 to 14 carbon atoms, Alk and Alk' are alkyl of 1 to 6 carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts with the proviso that when X is 8-CF3, R1 and R3 are hydrogen, R2 is 2-thiazolyl, R4 is methyl, R5 is not methyl having analgesic and anti-inflammatory activity.
机译: I的4-羟基-3-喹啉-羧酸盐的新型旋光异构体和外消旋物,其中X位于5-,6-,7-或8-位,并且选自氢,卤素,1至5个碳原子的烷基,1至4个碳原子的烷氧基,-CF 3,-SCF 3和-OCF 3,R 1选自氢和1至4个碳原子的烷基,R 2选自由噻唑基,4,5-二氢噻唑基,吡啶基,恶唑基,异恶唑基,咪唑基,嘧啶基和四唑基组成,它们均可选地被1-4个碳原子的烷基取代,并且苯基被至少一个由-OH,烷基和1-4个碳原子的烷氧基,-CF3,-NO2和卤素,R3和R4分别选自氢,1-4个碳原子的烷基和芳基,R5选自6的芳基碳原子数为14至14,碳原子数为3至14的杂芳基,碳原子数为1至14的烷基,烷基用-NH2,-NHAlk或2至6个碳原子的烯基,被6至14个碳原子的芳基取代的2至6个碳原子的烯基,Alk和Alk'表示的是1至6个碳原子的烷基无毒的药学上可接受的酸加成盐,条件是当X为8-CF3时,R1和R3为氢,R2为2-噻唑基,R4为甲基,R5不是具有镇痛和抗炎活性的甲基。

著录项

  • 公开/公告号ES8800162A1

    专利类型

  • 公开/公告日1987-11-01

    原文格式PDF

  • 申请/专利权人 ROUSSEL-UCLAF;

    申请/专利号ES19860556096

  • 发明设计人

    申请日1986-06-16

  • 分类号C07D215/56;A61K31/47;

  • 国家 ES

  • 入库时间 2022-08-22 07:17:02

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号