首页> 外国专利> NOVEL DERIVATIVES OF 3-BROMO- AND 3,3 DIBROMO-4-OXO-1-AZETIDINES, PROCESS FOR THE PREPARATION THEREOF AND THEIR USE

NOVEL DERIVATIVES OF 3-BROMO- AND 3,3 DIBROMO-4-OXO-1-AZETIDINES, PROCESS FOR THE PREPARATION THEREOF AND THEIR USE

机译:3-溴和3,3-二溴-4-氧代-1-氮杂环丁烷的新颖衍生物,其制备方法和用途

摘要

The invention relates to derivatives of 3-bromo- and 3,3-dibromo-4-oxo-1-azetidines of general formula I to processes for the preparation thereof and the use thereof. CHEM wherein CHEM wherein R4 is hydrogen, methyl, benzyl or some other protective group, R5 is hydrogen, alkyl, alkylaryl, a heterocyclic ring, Y is halo atom, X is halo atom, alkoxy group, nitroxy group. According to the invention derivatives of 3-bromo- and 3,3-dibromo-4-oxo-1-azetidines are prepared by the reaction of 2-sulfinic acid derivatives, preferably 2-substituted sulfinamides of 4-oxo-azetidines with various halogenating agents, and after the treatment of the reaction mixture, 2-halo derivatives of 3-bromo- and 3,3-dibromo-4-oxo-azetidines are isolated and are subjected to a reaction with silver tetrafluoroborate and alcohols to give the corresponding 2-alkoxy derivatives of 3-bromo- and 3,3-dibromo-4-oxo azetidines, or 2-halo derivatives of 3-bromo- and 3,3-dibromo-4-oxo azetidines are subjected to a reaction with silver nitrate in 2-propanol to give, after the treatment of the reaction mixture, 2-nitroxy derivatives of 3-bromo and 3,3-dibromo-4-oxo-1-azetidines. Some newly prepared compounds are deprotected and derivatives having a free carboxy group are obtained. The prepared compounds are components in pharmaceutical compositions effective in antibacterial or antitumour therapy.
机译:本发明涉及通式I的3-溴-和3,3-二溴-4-氧代-1-氮杂环丁烷的衍生物及其制备方法和用途。 ,其中其中R4是氢,甲基,苄基或一些其他保护基,R5是氢,烷基,烷基芳基,杂环,Y是卤原子,X是卤原子,烷氧基,硝基氧基。根据本发明,通过2-亚磺酸衍生物,优选4-氧代-氮杂环丁烷的2-取代的亚磺酰胺与各种卤化的反应来制备3-溴和3,3-二溴-4-氧代-1-氮杂环丁烷的衍生物。处理反应混合物后,分离出3-溴和3,3-二溴-4-氧杂氮杂环丁烷的2-卤代衍生物,并使其与四氟硼酸银和醇反应,得到相应的2 3-溴和3,3-二溴-4-氧杂环丁烷的2-烷氧基衍生物,或3-溴和3,3-二溴-4-氧杂环丁烷的2-卤衍生物与硝酸银反应处理反应混合物后,用2-丙醇制得3-溴和3-,3-二溴-4-氧代-1-氮杂环丁烷的2-硝基氧基衍生物。将一些新制备的化合物脱保护并获得具有游离羧基的衍生物。所制备的化合物是对抗菌或抗肿瘤治疗有效的药物组合物中的组分。

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