(I). ;The proposed method involves ortho-phenylenediamine condensing with bromocyanide, followed by bromohydrate removal with sodium carbonate and a reaction of obtained base transribosylation with uridine in the presence of catalytic amounts of uridine phosphorylase and purine nucleoside phosphorylase.;EFFECT: new effective anti-herpes virus compound is proposed, including that against variants of the virus resistant to the action of basic antiherpetic drugs, as well as a new effective method for obtaining.;3 cl, 3 ex, 4 dwg"/> 2-AMINO-5,6-DIFLUOR-1-(BETA-D-RIBOFURANOSYL)-BENZIMIDAZOLE, METHOD FOR PRODUCTION AND ANTIVIRAL ACTIVITY IN TERMS OF HERPES SIMPLEX VIRUS TYPE I
首页> 外国专利> 2-AMINO-5,6-DIFLUOR-1-(BETA-D-RIBOFURANOSYL)-BENZIMIDAZOLE, METHOD FOR PRODUCTION AND ANTIVIRAL ACTIVITY IN TERMS OF HERPES SIMPLEX VIRUS TYPE I

2-AMINO-5,6-DIFLUOR-1-(BETA-D-RIBOFURANOSYL)-BENZIMIDAZOLE, METHOD FOR PRODUCTION AND ANTIVIRAL ACTIVITY IN TERMS OF HERPES SIMPLEX VIRUS TYPE I

机译:I型疱疹病毒I型术语的2-氨基-5,6-二氟-1-(BETA-D-呋喃核糖基)-苯并咪唑的生产方法和抗病毒活性

摘要

FIELD: pharmacology.;SUBSTANCE: invention relates to a 2-amino-5,6-difluoro-1-(beta-D-ribofuranosyl)-benzimidazole of formula (I) suitable for treatment of herpes, and a method for its preparation that can be used in the pharmaceutical industry: ; (I). ;The proposed method involves ortho-phenylenediamine condensing with bromocyanide, followed by bromohydrate removal with sodium carbonate and a reaction of obtained base transribosylation with uridine in the presence of catalytic amounts of uridine phosphorylase and purine nucleoside phosphorylase.;EFFECT: new effective anti-herpes virus compound is proposed, including that against variants of the virus resistant to the action of basic antiherpetic drugs, as well as a new effective method for obtaining.;3 cl, 3 ex, 4 dwg
机译:发明领域本发明涉及适用于治疗疱疹的式(I)的2-氨基-5,6-二氟-1-(β-D-核呋喃糖基)-苯并咪唑及其制备方法,可用于制药行业: <图像文件=“ 00000009.JPG” he =“ 45” imgContent =“ undefined” imgFormat =“ JPEG” wi =“ 53” />(I)。 ;拟议的方法包括将邻苯二胺与溴氰化物缩合,然后用碳酸钠除去溴水合物,并在催化量的尿苷磷酸化酶和嘌呤核苷磷酸化酶的存在下,将尿嘧啶的碱基转移核糖基化反应。效果:新型有效的抗疱疹提出了一种新型的病毒化合物,包括针对抗基本抗疱疹药作用的病毒变种的化合物,以及一种新的有效获得方法。3 cl,3 ex,4 dwg

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