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AN IMPROVED PROCESS FOR THE PREPARATION OF AZILSARTAN MEDOXOMIL

机译:制备阿扎拉定莫多酚的改进方法

摘要

The present invention relates to an improved process for the preparation of azilsartan or its esters or salts thereof. Specifically, the invention provides a method for the preparation of highly pure methyl 1-[[2-(4,5-dihydro-5-oxo-4H-1,2,4-oxa-diazol-3-yl)biphenyl-4-yl]methyl]-2-ethoxy-1H-benzimidazole-7-carboxylate an intermediate compound of formula (4) for azilsartan medoxomil with reduced content of desethyl impurity. The invention also involves the use of highly pure methyl 1-[[2-(4,5-dihydro-5-oxo-4H-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl]-2-ethoxy-1H-benzimidazole-7-carboxylate in the preparation of azilsartan or its esters or salts thereof, preferably medoxomil with reduced content of desethyl impurity.
机译:本发明涉及制备阿齐沙坦或其酯或盐的改进方法。具体地说,本发明提供了一种制备高纯度甲基1-[[2-(4,5-二氢-5-氧代-4H-1,2,4-氧杂-二唑-3-基)联苯-4的方法。 -基]甲基] -2-乙氧基-1H-苯并咪唑-7-羧酸盐为式(4)的中间体化合物,用于阿齐沙坦美多米,其去乙基杂质含量降低。本发明还涉及使用高纯度的甲基1-[[2-(4,5-二氢-5-氧代-4H-1,2,4-恶二唑-3-基)联苯-4-基]甲基]-在制备阿齐沙坦或其酯或盐,优选为具有减少的去乙基杂质含量的美多沙美中,制备2-乙氧基-1H-苯并咪唑-7-羧酸盐。

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