摘要
A novel and practical synthetic route is presented for the preparation of methyl-（E）-2-（3-（3-（2-（7-chloro-2-quinolinyl）ethenyl） phenyl）-3-oxopropyl）benzoate,the key intermediate of Montelukast,a leukotriene antagonist.The main diarylpropane framework was prepared via a polarity conversation reaction resulting in an acyl anion equivalent followed by a nucleophilic substitution reaction.The overall yield of this approach was 61%.This method is simple for operation and suitable for industrial production.
A novel and practical synthetic route is presented for the preparation of methyl-（E）-2-（3-（3-（2-（7-chloro-2-quinolinyl）ethenyl） phenyl）-3-oxopropyl）benzoate,the key intermediate of Montelukast,a leukotriene antagonist.The main diarylpropane framework was prepared via a polarity conversation reaction resulting in an acyl anion equivalent followed by a nucleophilic substitution reaction.The overall yield of this approach was 61%.This method is simple for operation and suitable for industrial production.
基金
supported by the National Key Project for Basic Research(No2010CB1126102)
the Outstanding Youth Foundation of Heilongjiang Province(NoJC200706)
