首页> 外国专利> seen framstella aspirin - 3 - amino - 2 - hydroxibutyrylaminoettiksyror and even new intermediate products derfor and seen to framstella these

seen framstella aspirin - 3 - amino - 2 - hydroxibutyrylaminoettiksyror and even new intermediate products derfor and seen to framstella these

机译:看到了阿司匹林的阿司匹林-3-氨基-2-羟基丁酰氨基烟酰胺,甚至是新的中间体derfor,并看到了阿司匹林。

摘要

A process for producing threo-3-amino-2-hydroxybutanoylaminoacetic acids comprises the steps of allowing to react a starting compound represented by the general formula: IMAGE (I) wherein R1 represents a naphthyl or a group of the formula: IMAGE in which R6 and R7 represent individually hydrogen, halogen, amino or a protected amino, hydroxy or a protected hydroxy, a lower alkoxy or a lower alkyl and R2 represents a protected amino, with a starting compound represented by the general formula: IMAGE (II) wherein R3 represents hydrogen or an ester residue, to obtain threo-3-protected amino-2-hydroxy-4-oxobutanoic acid or its ester represented by the general formula: IMAGE (III) wherein R1, R2 and R3 have the same meanings as above, and then reducing the same into threo-3-protected amino-2-hydroxybutanoic acid or its ester represented by the general formula: IMAGE (IV) wherein R1, R2 and R3 have the same meanings as above, and further converting the above compound into 3-amino-2-hydroxybutanoic acid represented by the general formula: IMAGE (V) wherein R2' represents amino or a protected amino, thereafter condensing the same, in a conventional manner for forming a peptide coupling, with a compound represented by the general formula: IMAGE (VI) wherein R4 represents an alkyl having 3-4 carbon atom or 3-guanidinopropyl, while previously protecting as required those groups not relevant to the reaction, and removing the protecting groups for the functional groups to produce threo-3-amino-2-hydroxybutanoylaminoacetic acids represented by the general formula: IMAGE (VII) wherein R1 and R4 have the same meanings as above. This invention also provides the compounds represented by the general formula (III) as novel intermediates for the above aimed compounds and a process for producing the intermediates.
机译:生产苏-3-氨基-2-羟基丁酰基氨基乙酸的方法包括使由通式:(I)表示的起始化合物反应的步骤,其中R1代表萘基或以下通式的基团: >其中R6和R7分别代表氢,卤素,氨基或被保护的氨基,羟基或被保护的羟基,低级烷氧基或低级烷基,R2代表被保护的氨基,其中起始化合物由通式表示: >(II),其中R 3代表氢或酯残基,以获得由通式:IM 3表示的巯基-3-保护的氨基-2-羟基-4-氧代丁酸或其酯。 R3具有与上述相同的含义,然后将其还原为由巯基3保护的氨基-2-羟基丁酸或其酯,由通式:(IV)表示,其中R1,R2和R3具有相同的含义。如上所述,并进一步转换上述系数缩合成通式为(V)的3-氨基-2-羟基丁酸,其中R2′代表氨基或被保护的氨基,然后以常规方式与化合物缩合以形成肽偶联。 <通式>(VI),其中R4代表具有3-4个碳原子的烷基或3-胍基丙基,同时根据需要预先保护与反应无关的那些基团,并除去官能团的保护基制备由通式:(VII)表示的苏-3-氨基-2-羟基丁酰基氨基乙酸,其中R 1和R 4具有与上述相同的含义。本发明还提供由通式(III)表示的化合物,作为上述目标化合物的新型中间体,以及制备该中间体的方法。

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