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torihuruorometansuruhoniruokishikarubon derivative and its manufacturing method

机译:鸟嘌呤类衍生物及其合成方法

摘要

For the Contracting states : BE, CH, DE, FR, GB, IT, LU, NL, SE 1. A process for preparing compounds of the formula I see diagramm : EP0117448,P21,F1 in which n = 1 or 2, R denotes, hydrogen, carboxy, carbamoyl, an optionally substituted aliphatic radical having 2-8 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms, an OR**4 or SR**4 radical in which R**4 represents an optionally substituted aliphatic radical having 1-4 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms or an optionally substituted heteroaromatic radical having 5-10 ring atoms, or an optionally substituted heteroaromatic radical having 5-10 ring atoms, R**1 denotes hydrogen, an optionally substituted aliphatic radical having 1-6 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted cycloaliphatic-aliphatic radical having 4-13 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms, an optionally substituted araliphatic radical having 7-16 carbon atoms, an optionally substituted heteroaromatic radical having 5-10 ring atoms or the side chain of an optionally protected naturally occuring alpha-amino acid, R**2 and R**3 are identical or different and denote hydrogen, an optionally substituted aliphatic radical having 1-6 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted cycloaliphatic-aliphatic radical having 4-12 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms or an optionally substituted araliphatic radical having 7-16 carbon atoms, which comprises reacting compounds of the formulae II ou III see diagramm : EP0117448,P22,F2 in which n, R, R**1, R**2 and R**3 have the abovementioned meanings, with compounds of the formulae IV or V see diagramm : EP0117448,P22,F3 in which R, R**1, R**2, R**3 and n have the abovementioned meanings, if desired eliminating ester groups by hydrolysis or if desired esterifying free carboxyl groups in a manner known per se. For the Contracting state : Austria 1. A process for preparing compounds of the formula see diagramm : EP0117448,P25,F1 in which n = 1 or 2, R denotes, carbamoyl, hydrogen, carboxy an optionally substituted aliphatic radical having 2-8 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms, an OR**4 or SR**4 radical in which R**4 represents an optionally substituted aliphatic radical having 1-4 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms or an optionally substituted heteroaromatic radical having 5-10 ring atoms, or an optionally substituted heteroaromatic radical having 5-10 ring atoms, R**1 denotes hydrogen, an optionally substituted aliphatic radical having 1-6 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted cycloaliphatic-aliphatic radical having 4-13 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms, an optionally substituted araliphatic radical having 7-16 carbon atoms, an optionally substituted heteroaromatic radical having 5-10 ring atoms or the side chain of an optionally protected naturally accuring alpha-amino acid, R**2 and R**3 are identical or different and denote hydrogen, an optionally substituted aliphatic radical having 1-6 carbon atoms, an optionally substituted cycloaliphatic radical having 3-9 carbon atoms, an optionally substituted cycloaliphatic-aliphatic radical having 4-12 carbon atoms, an optionally substituted aromatic radical having 6-12 carbon atoms or an optionally substituted araliphatic radical having 7-16 carbon atoms, which comprises reacting compounds of the formulae II or III see diagramm : EP0117448,P26,F2 in which n, R, R**1, R**2 and R**3 have the abovementioned meanings, with compounds of the formulae IV or V see diagramm : EP0117448,P26,F3 in which R, R**1, R**2, R**3 and n have the abovementioned meanings, if desired eliminating ester groups by hydrolysis or hydrogenolysis or if desired esterifying free carboxyl groups in a manner known per se.
机译:对于缔约国:BE,CH,DE,FR,GB,IT,LU,NL,SE1。制备式I化合物的方法参见示意图:EP0117448,P21,F1,其中n = 1或2,R表示氢,羧基,氨基甲酰基,具有2-8个碳原子的任选取代的脂族基,具有3-9个碳原子的任选取代的脂环族基,具有6-12个碳原子的任选取代的芳族基,OR ** 4或SR ** 4基团,其中R ** 4代表具有1-4个碳原子的可选被取代的脂族基团,具有6-12个碳原子的可选被取代的芳族基团或具有5-10个环原子的可选被取代的杂芳族基团,或具有5-10个环原子的任选取代的杂芳族基团,R ** 1表示氢,具有1-6个碳原子的任选取代的脂族基团,具有3-9个碳原子的任选取代的脂环族基团,具有4 13个碳原子,具有6-12个碳原子的可选取代的芳族基团,具有7-16个碳原子的可选取代的芳脂族基团,具有5-10个环原子的可选取代的杂芳族基团或可选保护的天然存在的α的侧链-氨基酸,R ** 2和R ** 3相同或不同,表示氢,具有1-6个碳原子的任选取代的脂族基,具有3-9个碳原子的任选取代的脂环族基团,任选取代的脂环族-包含式II或III的反应化合物的具有4-12个碳原子的脂族基团,具有6-12个碳原子的可任选取代的芳族基团或具有7-16个碳原子的可任选取代的芳脂族基团,请参见示意图:EP0117448,P22,其中n,R,R ** 1,R ** 2和R ** 3具有上述含义的F2,具有式IV或V的化合物请参见示意图:EP0117448,P22,F3其中R,R ** 1 , R ** 2,R ** 3和n具有上述含义,如果需要的话,通过水解消除酯基,或者如果需要的话,以本身已知的方式酯化游离羧基。缔约国:奥地利1.制备下式化合物的方法,请参见示意图:EP0117448,P25,F1,其中n = 1或2,R表示氨基甲酰基,氢,羧基是一个可选取代的具有2-8个碳的脂族基团原子,可取代的具有3-9个碳原子的脂环族基团,可取代的具有6-12个碳原子的芳族基团,OR ** 4或SR ** 4原子团,其中R ** 4表示可取代的具有1-4个碳原子,具有6-12个碳原子的任选取代的芳族基团或具有5-10个环原子的任选取代的杂芳族基团或具有5-10个环原子的任选取代的杂芳族基团,R ** 1表示氢,具有1-6个碳原子的可任选取代的脂族基,具有3-9个碳原子的可任选取代的环脂族基,具有4-13个碳原子的可任选取代的环脂族-脂族基,具有6-12个碳原子的取代的芳族基团,具有7-16个碳原子的可选被取代的芳脂族基团,具有5-10个环原子的可选被取代的杂芳族基团或可选被保护的天然积累的α-氨基酸的侧链R * * 2和R ** 3相同或不同,表示氢,具有1-6个碳原子的任选取代的脂族基,具有3-9个碳原子的任选取代的脂环族基,具有4-12个碳的任选取代的脂环族脂族基碳原子,具有6-12个碳原子的任选取代的芳族基团或具有7-16个碳原子的任选取代的芳脂族基团,其包含式II或III的反应化合物,参见图:EP0117448,P26,F2,其中n,R ,R ** 1,R ** 2和R ** 3具有上述含义,式IV或V的化合物参见图:EP0117448,P26,F3,其中R,R ** 1,R ** 2, R ** 3和n具有上述值所提及的含义,如果需要的话,通过水解或氢解消除酯基,或者如果需要的话,以本身已知的方式酯化游离羧基。

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