【药物名称】Bezafibrate, BM-15075, Befizal, Bezalip Retard, Cedur, Bezatol, Bezalip
化学结构式(Chemical Structure):
参考文献No.47836
标题:Phenoxyalkylcarbos鋟rederivate und Verfahren zur Herstellung derselben
作者:Witte, E.C.; et al. (Boehringer Ingelheim GmbH)
来源:DE 2149070; ZA 7206638
合成路线图解说明:

The benzoylation of tyramine (2-(p-hydroxyphenyl)ethylamine) (I) with 4-chlorobenzoyl chloride (II) in pyridine gives 4-(4-chlorobenzoylaminoethyl)phenol (III), which by condensation with ethyl alpha-bromoisobutyrate (IV) by means of K2CO3 in refluxing butanone affords ethyl alpha-[4-(4-chlorobenzoylaminoethyl)phenoxy]isobutyrate (V). Finally, this compound is hydrolyzed with KOH in dioxane - water.

参考文献No.800563
标题:Bezafibrate
作者:Casta馿r, J.; Thorpe, P.
来源:Drugs Fut 1978,3(4),258
合成路线图解说明:

The benzoylation of tyramine (2-(p-hydroxyphenyl)ethylamine) (I) with 4-chlorobenzoyl chloride (II) in pyridine gives 4-(4-chlorobenzoylaminoethyl)phenol (III), which by condensation with ethyl alpha-bromoisobutyrate (IV) by means of K2CO3 in refluxing butanone affords ethyl alpha-[4-(4-chlorobenzoylaminoethyl)phenoxy]isobutyrate (V). Finally, this compound is hydrolyzed with KOH in dioxane - water.

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