首页> 外国专利> PROCESS FOR PRODUCING NEW 11-SUBSTITUTED 5,11-DIHYDRO-6H-PYRIDO-SQUARE BRACKET-2,3-B-SQUARE BRACKET CLOSED-SQUARE BRACKET-1,4-SQUARE BRACKET CLOSED-BENZODIAZEPIN-6-ONES

PROCESS FOR PRODUCING NEW 11-SUBSTITUTED 5,11-DIHYDRO-6H-PYRIDO-SQUARE BRACKET-2,3-B-SQUARE BRACKET CLOSED-SQUARE BRACKET-1,4-SQUARE BRACKET CLOSED-BENZODIAZEPIN-6-ONES

机译:生产新的11替代5,11-二氢-6H-吡咯烷-方形支架-2,3-B-方形支架封闭-方形支架-1,4-方形支架封闭-苯并二氮杂苯-6-酮

摘要

Compounds of the formula IMAGE wherein R1 is alkyl of 3 to 12 carbon atoms; unsaturated aliphatic hydrocarbyl of 3 to 20 carbon atoms comprising 1 to 3 double bonds and/or one triple bond; phenyl(alkyl of 2 to 4 carbon atoms); methylenedioxybenzyl; chlorobenzyl; indan-5-ylmethyl; indan-3-ylmethyl; phenyl(alkenyl of 2 to 4 carbon atoms); cycloalkyl of 5 to 7 carbon atoms; (cycloalkyl of 3 to 10 carbon atoms)methyl; (methylcycloalkyl of 4 to 11 carbon atoms)methyl; morpholino(alkyl of 2 to 3 carbon atoms); pyrrolidino(alkyl of 2 to 3 carbon atoms); piperidino (alkyl of 2 to 3 carbon atoms); 4-methylpiperazino(alkyl of 2 to 3 carbon atoms); or, when R3 and/or R4 are methyl or ethyl, also methyl or ethyl; R2 is hydrogen, methyl or ethyl; and R3 and R4 are each hydrogen, methyl or ethyl; and non-toxic, pharmacologically acceptable acid addition salts thereof. The compounds as well as the salts are useful as anti-ulcerogenics and secretion inhibitors.
机译:的化合物,其中R1是3至12个碳原子的烷基;具有1至3个双键和/或一个三键的3至20个碳原子的不饱和脂族烃基;苯基(2-4个碳原子的烷基);亚甲基二氧基苄基;氯苄;茚满-5-基甲基;茚满-3-基甲基;苯基(2-4个碳原子的烯基); 5至7个碳原子的环烷基; (3至10个碳原子的环烷基)甲基; (4至11个碳原子的甲基环烷基)甲基;吗啉代(具有2至3个碳原子的烷基);吡咯烷基(碳原子数2至3的烷基);哌啶子基(具有2至3个碳原子的烷基); 4-甲基哌嗪子基(具有2至3个碳原子的烷基);当R 3和/或R 4为甲基或乙基时,也为甲基或乙基;或R 2是氢,甲基或乙基; R3和R4分别为氢,甲基或乙基;及其无毒的药理学上可接受的酸加成盐。所述化合物以及盐可用作抗溃疡药和分泌抑制剂。

著录项

  • 公开/公告号HU180999B

    专利类型

  • 公开/公告日1983-05-30

    原文格式PDF

  • 申请/专利权人 THOMAE GMBH DR KARL;

    申请/专利号HU1978TO01081

  • 发明设计人 SCHMIDTGUENTERDE;LEITOLDMATYASDE;

    申请日1978-05-30

  • 分类号C07D471/04;

  • 国家 HU

  • 入库时间 2022-08-22 11:09:32

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