首页> 外国专利> FOERFARANDE Før FRAMSTAELLNING audio TERAPEUTISKT ANVAENDBARA NYA 1,2,4-TRIAZOLO / 4.3 A / KINAZOLIN-5 (4H) -ONER OCH deras SALTER.

FOERFARANDE Før FRAMSTAELLNING audio TERAPEUTISKT ANVAENDBARA NYA 1,2,4-TRIAZOLO / 4.3 A / KINAZOLIN-5 (4H) -ONER OCH deras SALTER.

机译:在制造音频之前进行操作,然后以音响方式治疗性地使用新的1,2,4-TRIAZOLO / 4.3 A / KINAZOLIN-5(4H)及其盐。

摘要

Novel triazoloquinazolones of the formula IMAGE I wherein R and R' are individually selected from the group consisting of hydrogen, halogen, nitro and alkyl and alkoxy of 1 to 3 carbon atoms, Y is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 4 carbon atoms, cycloalkyl of 3 to 8 carbon atoms, aryl of 6 to 8 carbon atoms and aralkyl of 7 to 8 carbon atoms, B is an alkylene of 1 to 3 carbon atoms, X is selected from the group consisting of IMAGE R1 and R2 are individually selected from the group consisting of hydrogen, alkyl of 1 to 6 carbon atoms, cycloalkyl of 3 to 8 carbon atoms, aryl of 6 to 8 carbon atoms, aralkyl of 7 to 8 carbon atoms, aminoalkyl of 2 to 4 carbon atoms, mono- and dialkylaminoalkyl with each alkyl having 2 to 4 carbon atoms, piperidinoalkyl of 1 to 4 alkyl carbon atoms, morpholinoalkyl of 1 to 4 alkyl carbon atoms and piperazinylalkyl of 1 to 4 alkyl carbon atoms or R1 and R2 taken together with the nitrogen to which they are attached form a saturated mono- or bicyclic heterocyclic ring with 4 to 8 carbon atoms optionally substituted with 1 to 2 methyls and optionally containing in the ring a heteroatom selected from -O-, -S- and IMAGE and R3 is selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms, hydroxyalkyl of 1 to 3 carbon atoms, alkoxycarbonyl of 2 to 5 carbon atoms, aryl of 6 to 8 carbon atoms and aralkyl of 7 to 8 carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts having antihistaminic and bronchospasmolytic activity and their preparation and intermediates.
机译: I的新型三唑并喹唑啉酮,其中R和R'分别选自氢,卤素,硝基和烷基以及具有1至3个碳原子的烷氧基,Y选自由1至3个烷基组成的组6个碳原子,2-4个碳原子的烯基,3-8个碳原子的环烷基,6-8个碳原子的芳基和7-8个碳原子的芳烷基,B是1-3个碳原子的亚烷基,选择X R 1和R 2分别选自氢,碳原子数为1至6的烷基,碳原子数为3至8的环烷基,碳原子数为6至8的芳基,芳族烷基为7至8碳原子,具有2-4个碳原子的氨基烷基,每个烷基具有2-4个碳原子的单和二烷基氨基烷基,具有1-4个烷基碳原子的哌啶子基烷基,具有1-4个烷基碳原子的吗啉代烷基和具有1-4个烷基碳的哌嗪基烷基原子或R1和R2与氮一起生成h它们连接形成具有4至8个碳原子的饱和的单环或双环杂环,其任选地被1-2个甲基取代,并且在环中任选地包含选自-O-,-S-和的杂原子,并且R 3是选自氢,1-3个碳原子的烷基,1-3个碳原子的羟烷基,2-5个碳原子的烷氧羰基,6-8个碳原子的芳基和7-8个碳原子的芳烷基及其非取代基具有抗组胺和支气管痉挛活性的抗毒性,药学上可接受的酸加成盐及其制备方法和中间体。

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