首页> 外国专利> Process for Preparation of (1R, 5S, 6S) -2- 1- (1,3-Thiazolin-2-yl) azetidin-3-yl -thio-6 - (R) -1-hydroxyethyl -1 methylcarbapen-2-em-3-carboxylic acid derivatives

Process for Preparation of (1R, 5S, 6S) -2- 1- (1,3-Thiazolin-2-yl) azetidin-3-yl -thio-6 - (R) -1-hydroxyethyl -1 methylcarbapen-2-em-3-carboxylic acid derivatives

机译:(1R,5S,6S)-2- [1-(1-,1,3-噻唑啉-2-基)氮杂环丁烷-3-基]-硫基-6-[(R)-1-羟乙基] -1的制备方法甲基卡宾-2-em-3-羧酸衍生物

摘要

Novel carbapenem compounds, (1R,5S,6S)-2-[1-(1,3-thiazolin-2-yl)azetidin-3-yl]thio-6-[(R)-1-hydrox yethyl]-1-methyl-carbapen- 2-em-3-carboxyic acid derivatives. These carbapenem compounds are represented by the following formula having a beta-coordinated methyl group introduced at the 1-position and a [1-(1,3-thiazolin-2-yl)azetidin-3-yl]thio group introduced at the 2-position. CHEM In the formula, R is hydrogen; lower alkyl group which is unsubstituted or substituted by hydroxy, lower alkoxy or lower alkoxy-lower alkoxy group; group -COOR1 (R1 is hydrogen or lower alkyl group); or group -CONR2R3 (R2 and R3 are, independently each other, hydrogen or lower alkyl), and Y is carboxy, -COO(-) or protected carboxy. These compounds are useful antibiotics for prevention and treatment of bacterial infections.
机译:新型碳青霉烯化合物(1R,5S,6S)-2- [1-(1-(1,3-噻唑啉-2-基)氮杂环丁烷-3-基]硫基-6-[(R)-1-羟基丁] -1 -甲基-卡宾-2-em-3-羧酸衍生物。这些碳青霉烯化合物由下式表示,具有在1位引入的β-配位甲基和在2位引入的[1-(1,3-噻唑啉-2-基)氮杂环丁烷-3-基]硫基。 -位置。 <化学式>式中,R为氢。未取代或被羟基,低级烷氧基或低级烷氧基-低级烷氧基取代的低级烷基; -COOR 1基团(R 1为氢或低级烷基);或基团-CONR 2 R 3(R 2和R 3彼此独立地是氢或低级烷基),并且Y是羧基,-COO(-)或被保护的羧基。这些化合物是用于预防和治疗细菌感染的有用抗生素。

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