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首页> 外文期刊>Journal of chemical research: reviews and research papers from all branches of chemistry >Synthesis of a Benvitimod impurity: (Z)-3,5-dihydroxy-4-isopropylstilbene
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Synthesis of a Benvitimod impurity: (Z)-3,5-dihydroxy-4-isopropylstilbene

机译:Benvitimod杂质的合成:(Z)-3,5-二羟基-4-异丙基二苯乙烯

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摘要

(E)-3,5-dihydroxy-4-isopropylstilbene (Benvitimod), a new medicine for the treatment of psoriasis and eczema, belongs to the hydroxystilbene family. The synthesis leads to the E-isomer, (Z)-3,5-dihydroxy-4-isopropylstilbene being present as a major impurity in the preparation of Benvitimod. We describe a synthesis of the Benvitimod impurity: (Z)-3,5-dihydroxy-4-isopropylstilbene starting from 3,5-dihydroxybenzoic acid, through an isopropyl reaction, esterification and etherification, reduction, oxidation, Perkin condensation, decarboxylation and demethylation. The optimal reaction conditions were also determined.
机译:(E)-3,5-dihydroxy-4-isopropylstilbene(Benvitimod)是一种治疗牛皮癣和湿疹的新药物,属于hydroxystilbene家族。合成导致E-异构体,(Z)-3,5-二羟基-4-异丙基sti作为苯甲醇的制备中的主要杂质存在。我们描述了Benvitimod杂质的合成:通过异丙基反应,酯化和醚化,还原,氧化,珀金缩合,脱羧和脱甲基,从3,5-二羟基苯甲酸开始合成(Z)-3,5-二羟基-4-异丙基苯乙烯。还确定了最佳反应条件。

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