首页> 外国专利> ANTHRACYCLINE DERIVATIVES, METHOD OF PRODUCING 13-BENZENIDESULPHONYLHYDRAZINE DERIVATIVES OF ANTHRACYCLINES, METHOD OF PRODUCING 13-DEOXYANTHRACYCLINES, METHOD OF PRODUCING 5-IMINO-13-DEOXYANTHRACYCLINES

ANTHRACYCLINE DERIVATIVES, METHOD OF PRODUCING 13-BENZENIDESULPHONYLHYDRAZINE DERIVATIVES OF ANTHRACYCLINES, METHOD OF PRODUCING 13-DEOXYANTHRACYCLINES, METHOD OF PRODUCING 5-IMINO-13-DEOXYANTHRACYCLINES

机译:蒽环类衍生物,蒽环类化合物的13-苯甲磺酰基肼基衍生物的制备方法,十三-脱氧蒽环类化合物的制备方法,5-亚氨基-13-脱氧酞菁类化合物的制备方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to anthracycline derivatives of general structural formula given below ;where R1, R2 and R3 are H or OH; R4 denotes H, OH, C1-C5alkyl, or O-(C1-C5)alkyl; R5 is O or NH; and R6 is selected from a group comprising H, OH and a sugar residue which is The invention also relates to a method of producing said derivatives by reacting 13-ketoanthracycline or acid salt thereof with benzenidesulphonylhydrazide in an alcohol solvent at temperature of approximately 35-50°C for approximately 10-24 hours. The invention also pertains to a method of producing 13-deoxyanthracyclines, involving preparation of an alcoholic solution of the said 13-benzenidesulphonylhydrazine anthracycline; addition of a reducing agent and acid to the said solution; heating said solution without stirring, agitation or dephlegmation in order to reduce said 13-benzenidesulphonylhydrazine anthracycline; neutralisation of said solution with an aqueous solution of a base to obtain said 13-deoxyanthracycline derivative and precipitation; and, additionally, filtration of said precipitate, extraction of said 13-deoxyanthracycline from said precipitate, as well as extraction of said 13-deoxyanthracycline from the filtrate. The invention also relates to a method of producing 5-imino-13-deoxyanthracyclines involving synthesis of 13-deoxyanthracyclines as described above; dissolution of said 13-deoxyanthracyclines in an alcohol and conversion of said 13-deoxyanthracyclines to the corresponding 5-imino-13-deoxyanthracyclines under the effect of ammonia at temperature lower than approximately 20°C. The invention also relates to a method of producing 13-deoxyanthracyclines involving preparation of an alcoholic solution of 13-benzenidesulphonylhydrazine anthracycline having structural formula given below; addition of a reducing agent and a pyridinium acid salt to the said solution and heating said solution to reduce said 13-benzenidesulphonylhydrazine anthracycline. The invention also relates to a method of producing 5-imino-13-deoxyanthracyclines involving preparation of said 13-deoxyanthracycline and its conversion to the corresponding 5-imino-13-deoxyanthracycline under the effect of ammonia at temperature lower than approximately 20°C.;EFFECT: new compounds have useful biological properties.;21 cl, 4 tbl, 4 ex
机译:发明领域本发明涉及下面给出的通用结构式的蒽环衍生物。;其中R 1 ,R 2 和R 3 是H或OH; R 4 表示H,OH,C 1 -C 5 烷基或O-(C 1 -C 5 )烷基; R 5 是O或NH; R 6 选自H,OH和糖残基,该残基为本发明还涉及通过在醇溶剂中在约35-50°C的温度下使13-酮蒽环类或其酸盐与苯甲酰磺酰肼反应约10-24小时来制备所述衍生物的方法。本发明还涉及一种生产13-脱氧蒽环霉素的方法,该方法包括制备所述13-苯甲酰胺基磺酰肼蒽环霉素的醇溶液。向所述溶液中添加还原剂和酸;加热所述溶液而不搅拌,搅动或除痰,以减少所述13-苯甲磺酰基肼蒽环霉素;用碱的水溶液中和所述溶液,得到13-脱氧蒽环衍生物并沉淀。另外,过滤所述沉淀物,从所述沉淀物中提取所述13-脱氧蒽环,以及从滤液中提取所述13-脱氧蒽环。本发明还涉及一种生产5-亚氨基-13-脱氧蒽环霉素的方法,该方法涉及如上所述的13-脱氧蒽环霉素的合成。在低于约20℃的温度下,在氨的作用下,将所述13-脱氧蒽环胺溶解在醇中并将所述13-脱氧蒽环胺转化为相应的5-亚氨基-13-脱氧蒽环胺。本发明还涉及一种制备13-脱氧蒽环霉素的方法,该方法包括制备具有以下结构式的13-苯甲酰磺酰基肼蒽环蒽的醇溶液;向所述溶液中加入还原剂和吡啶鎓酸盐,并加热所述溶液以还原所述13-苯甲磺酰肼蒽蒽环。本发明还涉及一种生产5-亚氨基-13-脱氧蒽环的方法,该方法包括制备所述13-脱氧蒽环并在低于约20℃的温度下在氨的作用下将其转化为相应的5-亚氨基-13-脱氧蒽环。效果:新化合物具有有用的生物学特性。; 21 cl,4 tbl,4 ex

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